About: Ron A. Wevers

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl)
rdfs:label	Ron A. Wevers (de) Ron A. Wevers (en) Ron A. Wevers (es) Ron A. Wevers (fr) Ron A. Wevers (nl) Ron A. Wevers (sl) Ron A. Wevers (ast)
skos:prefLabel	Ron A. Wevers (de) Ron A. Wevers (en) Ron A. Wevers (es) Ron A. Wevers (fr) Ron A. Wevers (nl) Ron A. Wevers (sl) Ron A. Wevers (ast)
name	Ron A. Wevers (de) Ron A. Wevers (en) Ron A. Wevers (es) Ron A. Wevers (fr) Ron A. Wevers (nl) Ron A. Wevers (sl) Ron A. Wevers (ast)
given name	wds:Q42739481-360D2563-5185-4881-B53C-65926AC3DA52
given name	Ron
instance of	wds:Q42739481-C34C9729-F8BA-4D78-B457-8794D65C0D07
instance of	Homo sapiens
skos:altLabel	Ron Wevers (en) RA Wevers (en)
Nationale Thesaurus voor Auteursnamen ID	wds:Q42739481-a91f39df-32b5-4a34-aaff-81e545d49ed0
occupation	wds:Q42739481-65D7B206-6893-4421-8D14-BF21EEECCC45
employer	wds:Q42739481-6EEB8638-420E-43C4-B00F-2BFB49D1D2D4
NUKAT ID	wds:Q42739481-D1A85000-B945-4FE7-8D42-8A91A8D8CA52
sex or gender	wds:Q42739481-cb47004b-4e10-8b76-7796-a0063fb823c7
ISNI	wds:Q42739481-71480207-E840-4F14-9538-7C4B05B34542
VIAF ID	wds:Q42739481-47B9F1CE-58FB-47B2-950E-10422E165261
GND ID	wds:Q42739481-9613d5b4-8005-4acf-a8ca-9d5942bab61a
Library of Congress authority ID	wds:Q42739481-F4B59BF8-AE8A-478A-931A-3D3F61895182
IdRef ID	wds:Q42739481-5ba10006-76c1-497f-9f0e-1e97486679cc
date of birth	wds:Q42739481-528B877A-6C07-4DFB-8B55-35C58DF3C20F
WorldCat Identities ID (superseded)	wds:Q42739481-F43B947B-CDA2-4931-99EE-924656A77896
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p068311508
VIAF ID	http://viaf.org/viaf/236610377
GND ID	https://d-nb.info/gnd/1029526869
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2012183546
IdRef ID	http://www.idref.fr/225894629/id
Nationale Thesaurus voor Auteursnamen ID	068311508
occupation	researcher
employer	Radboud University Medical Centre
NUKAT ID	n2014082875
sex or gender	male
ISNI	0000000370348275
VIAF ID	236610377
GND ID	1029526869
Library of Congress authority ID	n2012183546
IdRef ID	225894629
date of birth	1951-01-01 00:00:00Z (xsd:dateTime)
WorldCat Identities ID (superseded)	lccn-n2012183546
ORCID iD	wds:Q42739481-31E35B82-22B6-40D9-9DE0-FBC18012B03B
ORCID iD	https://orcid.org/0000-0003-2278-9746
ORCID iD	0000-0003-2278-9746
ResearcherID	wds:Q42739481-B84B27B8-B11D-4778-929F-8C7277DE5B70
Publons author ID	wds:Q42739481-4eefae00-f7cf-4777-a56d-ede03a177f2a
ResearcherID	H-8116-2014
Publons author ID	2513561
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42739481
is author of	Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiency Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype. Lactobacilli and acidosis in children with short small bowel NMR spectroscopic studies on the late onset form of 3-methylglutaconic aciduria type I and other defects in leucine metabolism. Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome) cDNA cloning, genomic structure and chromosomal localization of the human BUP-1 gene encoding beta-ureidopropionase Protein complexes in the archaeon Methanothermobacter thermautotrophicus analyzed by blue native/SDS-PAGE and mass spectrometry Aminoacylase I deficiency: a novel inborn error of metabolism. The relation between blood lactate and ammonia in ischemic handgrip exercise Elevated plasma chitotriosidase activity in various lysosomal storage disorders. Apolipoprotein C-III isofocusing in the diagnosis of genetic defects in O-glycan biosynthesis Arts syndrome is caused by loss-of-function mutations in PRPS1 SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. beta-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities Dopa-responsive dystonia: A clinical and molecular genetic study beta-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brain. The frequency of lysosomal storage diseases in The Netherlands.

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