Query author contributions in Reactome

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Details on Person Wilcox, WR

Class:Id	Person:194685
_displayName	Wilcox, WR
_timestamp	2007-03-22 15:07:41
created	[InstanceEdit:194683] D'Eustachio, P, 2007-03-22 16:07:19
firstname	William R
initial	WR
surname	Wilcox
(author)	[LiteratureReference:194732] Autosomal recessive HEM/Greenberg skeletal dysplasia is caused by 3 beta-hydroxysterol delta 14-reductase deficiency due to mutations in the lamin B receptor gene [LiteratureReference:195694] Mutations in the gene encoding 3 beta-hydroxysteroid-delta 8, delta 7-isomerase cause X-linked dominant Conradi-Hunermann syndrome [LiteratureReference:2002426] Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene [LiteratureReference:2032916] A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene [LiteratureReference:2054054] Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3 [LiteratureReference:2060834] Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3 [LiteratureReference:2065481] NF449 is a novel inhibitor of fibroblast growth factor receptor 3 (FGFR3) signaling active in chondrocytes and multiple myeloma cells [LiteratureReference:2470656] Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene [LiteratureReference:3621693] Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene
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No pathways have been reviewed or authored by Wilcox, WR (194685)