WAS |
Wiskott-Aldrich syndrome (eczema-thrombocytopenia) |
300392 |
WASbase: Mutation registry for Wiskott-Aldrich syndrome (WAS) |
Mauno Vihinen, Univ. of Tampere, Tampere, Finland |
WAS |
Wiskott-Aldrich syndrome (eczema-thrombocytopenia) |
300392 |
CCHMC - Human Genetics Mutation Database |
Ammar Husami and Theru A. Sivakumaran |
WDR13 |
WD repeat domain 13 |
300512 |
WDR13 database at LOVD |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
WDR44 |
WD repeat domain 44 |
\N |
WDR44 database at LOVD |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
WFS1 |
Wolfram syndrome 1 (wolframin) |
606201 |
Hereditary Hearing Loss Homepage |
Guy van Camp, Univ. of Antwerp, Antwerp, Belgium; Richard J.H. Smith, Univ. of Iowa Hospitals & Clinics, Iowa city, U.S.A |
WFS1 |
Wolfram syndrome 1 (wolframin) |
606201 |
CCHMC - Human Genetics Mutation Database |
Ammar Husami and Theru A. Sivakumaran |
WFS1 |
Wolfram syndrome 1 (wolframin) |
606201 |
EURO-WABB Project Open Variation Database |
Dewi Astuti |
WNK1 |
WNK lysine deficient protein kinase 1 |
608620 |
Inherited Peripheral Neuropathies Mutation Database |
Eva Nelis, Molecular Genetics Department, Flanders Interuniversity Institute for Biotechnology (VIB), University of Antwerp (UA), Belgium |
WNK3 |
WNK lysine deficient protein kinase 3 |
300358 |
WNK3 database at LOVD |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |
WRAP53 |
WD repeat containing, antisense to TP53 |
612661 |
The Telomerase Database |
Julian J-L Chen at Arizona State University |
WRN |
Werner syndrome, RecQ helicase-like |
604611 |
Database of WS-associated WRN mutations |
International Registry of Werner Syndrome, George M. Martin, Junko Oshima & Dru F. Leistritz, Department of Pathology, University of Washington, Seattle, USA |
WWC3 |
WWC family member 3 |
\N |
WWC3 database at LOVD |
Johan T. den Dunnen Leiden Univ. Med Centre (acting), Curator vacancy |