About: A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement

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About: A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement Goto Sponge NotDistinct Permalink

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scientific article published on 01 May 1996

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 1996 (uk) im Mai 1996 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en mayu de 1996 (ast) scientific article published on 01 May 1996 (en)
publication date	wds:Q71053676-21FA2508-C8EE-4296-AAAD-AD600690EE62
publication date	1996-05-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q71053676-1D5CBA90-5850-47CE-8E94-CAA85A9766D0 wds:Q71053676-33D80703-3D28-44E6-83AC-96A3307BE548 wds:Q71053676-51785D01-E146-4C34-B783-26FC7422428F wds:Q71053676-6121AC02-41D9-44BF-BEFD-2F97EDA1CF20 wds:Q71053676-7DA830E4-B45A-4A9A-A482-1CD810B60E44 wds:Q71053676-816B96CD-D92A-4F86-902F-30CB0F59BDD8 wds:Q71053676-8819C48F-8881-4DC5-8AB5-1AE297C0F6CB wds:Q71053676-D45C9427-CF30-4D79-9466-4410D088EE3E wds:Q71053676-EE8335E5-102D-49F3-8244-D680FA9C38DC
author name string	Becker AE de Visser M Troost D Busch HF Bouwsma G de Voogt WG van der Kooi AJ Ledderhof TM Res CJ
rdfs:label	A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (en) A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (nl)
skos:prefLabel	A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (en) A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (nl)
name	A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (en) A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (nl)
title	wds:Q71053676-1D7E639C-A5FD-41CA-A79A-0599696A0F2C
title	A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement (en)
page(s)	wds:Q71053676-AE93C644-0BC9-4921-B637-371B4DCD6335
page(s)	636-642
instance of	wds:Q71053676-EB11AC66-A36E-4B1C-8EB4-3C06592F81D6
instance of	scholarly article
main subject	wds:Q71053676-F91E5169-9D7C-469A-92C6-E8BC19B77721
main subject	autosomal dominant limb-girdle muscular dystrophy
PubMed ID	wds:Q71053676-E40FADA5-862A-4B7B-8A5F-DC956D65D9BA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8619549
PubMed ID	8619549
published in	wds:Q71053676-89CEB6CA-D768-48A3-8331-76F055785DD9
published in	Annals of Neurology
issue	wds:Q71053676-15B1AABD-7A12-402A-A09A-3B7A9BA511CE
volume	wds:Q71053676-6DC3C7CB-3F79-4CEE-9547-93703BC28F4C
issue	5
volume	39
DOI	wds:Q71053676-BF1FE546-9E6D-4A79-AAC4-C48CB76EFDC1
DOI	http://dx.doi.org/10.1002/ANA.410390513
DOI	10.1002/ANA.410390513
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q71053676
is cites work of	The inner nuclear membrane protein emerin regulates beta-catenin activity by restricting its accumulation in the nucleus Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A/C gene A missense mutation in the exon 8 of lamin A/C gene in a Japanese case of autosomal dominant limb-girdle muscular dystrophy and cardiac conduction block Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Laminopathies: multisystem dystrophy syndromes The heart in limb girdle muscular dystrophy. Cardiac arrhythmias as presenting symptoms in patients with limb-girdle muscular dystrophy Autosomal dominant Emery-Dreifuss muscular dystrophy: a new family with late diagnosis Cardiac dysrhythmias,cardiomyopathy and muscular dystrophy in patients with Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy type 1B. Primate genome gain and loss: a bone dysplasia, muscular dystrophy, and bone cancer syndrome resulting from mutated retroviral-derived MTAP transcripts. Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins Diseases of the Nucleoskeleton. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. Correlation of metastasis-related gene expression with metastatic potential in human prostate carcinoma cells implanted in nude mice using an in situ messenger RNA hybridization technique Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death? Management of cardiac complications in neuromuscular disease. [Cardiac involvement in neuromuscular diseases] Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21. Advances in basic and clinical research in laminopathies Early-Onset LMNA-Associated Muscular Dystrophy with Later Involvement of Contracture Pacing for conduction disturbances in Steinert's disease: a new indication for biventricular ICD? Cardioembolic stroke related to limb-girdle muscular dystrophy 1B. Klinik und Genetik der Gliederg�rteldystrophien Myopathies with early contractures
is cites work of	wds:Q28188458-28CFE78E-3EB6-4388-9CFE-2B0909EF5FDA wds:Q33599572-6591B57E-22FA-4674-A2B9-98D4832BC578 wds:Q36346720-D94626EB-658C-4E8C-B8C3-0E2B9A8F91E2 wds:Q22009039-A5DD2709-0BE2-42AD-834C-9A5226B508F1 wds:Q35954331-4A89CDD0-D5AD-469C-9D02-EAAF545A22B3 wds:Q61647740-6467A17C-5F4A-4007-8234-A2338471C4E0 wds:Q24297804-916A78E5-0AD3-46FC-BC7A-238A8EE729EF wds:Q35589666-70D34C22-1A28-43F5-A085-9EBA622F8828 wds:Q42646112-FF927FE6-36CB-42EB-AB91-8AE573C6C4AA wds:Q30666516-46AC2F82-E192-40CC-B81A-A14F9C1E35D6 wds:Q45242479-94F9E75E-2475-4A3E-A266-88C9FE66C5A3 wds:Q63531531-45F2FBFB-BA20-402C-A285-EFF559E8A3C1 wds:Q34567041-D28FCFE2-F06A-4373-B493-2638DE727114 wds:Q35238579-63900112-140E-4E71-AFA5-42056DDDBBF4 wds:Q35764474-4C440933-0ACA-47F1-88B4-D52F6359997B wds:Q38991463-03F39ADE-7CDF-461B-925E-7A3F69C517CC wds:Q56459995-B48330C6-E358-4C7A-82E4-8750255D04C9 wds:Q35249710-9B87C381-2E96-4026-A446-170726335ABF wds:Q42034492-2E056B0B-B060-4C04-BBBA-2B5B802D9960

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