About: Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV.

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About: Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. Goto Sponge NotDistinct Permalink

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scientific article published on August 2007

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2007 (ast) наукова стаття, опублікована в серпні 2007 (uk) مقالة علمية نشرت في أغسطس 2007 (ar) scientific article published on August 2007 (en)
publication date	wds:Q37221113-F5D73BCC-487C-4182-AEF0-F83851EF710F
publication date	2007-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37221113-B96B3D83-C6AC-4F32-9704-B97315B38775
language of work or name	English
cites work	wds:Q37221113-1F114C11-B910-47C5-85CE-B67725637CD7 wds:Q37221113-1F4D3FE4-AAF4-45A3-B23C-F5BCF9C2F8FE wds:Q37221113-206AD12B-CD37-4BAA-B4BE-DA9E2A5751FE wds:Q37221113-2C8FE163-578A-487F-BB55-3F4612504C12 wds:Q37221113-37615521-2F77-4053-AFD5-A1295D5CD776 wds:Q37221113-6376F0E2-8282-4345-9B09-64A862200CE5 wds:Q37221113-A09E89ED-F904-452D-955E-E9AC0C02A319 wds:Q37221113-B0FE230B-1DCC-48E3-85F1-5B60ABDC302A wds:Q37221113-C6B7F248-C673-4007-B390-5871D81C96CD wds:Q37221113-FCF2363E-BD00-41DA-97CA-696FB11F9733
cites work	Spontaneous direct carotid-cavernous fistula in Ehlers-Danlos syndrome type IV: two case reports and a review of the literature Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type Aneurysm syndromes caused by mutations in the TGF-beta receptor Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK). A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 Vascular Ehlers-Danlos syndrome. Cerebrovascular complications in Ehlers-Danlos syndrome type IV. Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome The Ehlers-Danlos syndrome: a heritable collagen disorder as cause of bleeding. Skin manifestations, multiple aneurysms, and carotid-cavernous fistula in Ehlers-Danlos syndrome type IV
author name string	wds:Q37221113-1460B4CE-7932-4B0E-BE0D-6AF089AF8388 wds:Q37221113-2722323D-544B-4409-9016-456AF287054E wds:Q37221113-6D610E10-C5A4-4843-B7FA-886D8086CF84 wds:Q37221113-7BB5C5AD-135B-4322-B7F5-FA9C3BEAE41F wds:Q37221113-AD663765-1CB0-46B7-8FB9-41A386203D30 wds:Q37221113-F4610638-1A33-40C4-9C27-1E0CF4A41CB4
author name string	Jeong Hoon Yang Duk Kyung Kim Shin Yi Jang Chang Seok Ki Sung Hae Kim Jee Ah Kim
rdfs:label	Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (en) Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (nl) Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (ast)
skos:prefLabel	Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (en) Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (nl) Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (ast)
name	Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (en) Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (nl) Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV. (ast)
author	wds:Q37221113-EFB71783-726C-4431-8727-D0740C4563A7
author	Seung-Tae Lee
title	wds:Q37221113-826509BA-9136-4CAB-9CBA-8CC055D211DF
title	Genetic analysis of three Korean patients with clinical features of Ehlers-Danlos syndrome type IV (en)
page(s)	wds:Q37221113-982FC8C6-5A47-4D46-89C8-527486D613DA
page(s)	698-705
instance of	wds:Q37221113-239E78B3-2371-4B0E-8737-091362B681C2
instance of	scholarly article
main subject	wds:Q37221113-5385c760-b60a-4471-b74c-399ced32798c
main subject	Ehlers-Danlos syndrome
PubMed ID	wds:Q37221113-3C14F1BC-FCCE-4501-9217-2E9909D129E6
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17728513
PubMed ID	17728513
published in	wds:Q37221113-F349ECBF-4403-4C64-91A7-AF9D3415358C
published in	Journal of Korean Medical Science
issue	wds:Q37221113-8995A2D2-3A9B-4A43-B65D-B3BC4C136325
volume	wds:Q37221113-01CC5616-56B2-4D4E-A2AB-C2B0D83D6861
issue	4
volume	22
DOI	wds:Q37221113-B0283A9F-C58F-4BFF-9C73-AA114C71DF4A
DOI	http://dx.doi.org/10.3346/JKMS.2007.22.4.698
DOI	10.3346/JKMS.2007.22.4.698
copyright license	wds:Q37221113-05463137-c6a3-4ded-b0a7-0759cedb9506
copyright status	wds:Q37221113-2af602a9-de07-4fcc-b362-3296db589f52
copyright license	Creative Commons Attribution-NonCommercial 3.0 Unported
copyright status	copyrighted
ResearchGate publication ID	wds:Q37221113-52221B87-F545-4657-B1D3-1CA4DE5196C5
ResearchGate publication ID	6111047
PMCID	wds:Q37221113-7DFBECB9-338E-4018-B797-DCF8F95B75DD
PMCID	2693823
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37221113
is cites work of	Sigmoid colon perforation induced by the vascular type of Ehlers-Danlos syndrome: report of a case. Occlusive vascular Ehlers-Danlos syndrome accompanying a congenital cystic adenomatoid malformation of the lung: report of a case. Clinical features and genetic analysis of Korean patients with Loeys-Dietz syndrome Pathophysiology of carotid-cavernous fistulas in vascular Ehlers-Danlos syndrome: a retrospective cohort and comprehensive review.
is cites work of	wds:Q50538409-593AFF18-D602-4B74-9703-553AE5F59FC1 wds:Q44015838-63BF0C04-0D74-4C8D-BDFB-6FF871C4AF94 wds:Q38457577-F6593C21-7284-48C6-BC66-F6E042480FB9

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