jueves, 3 de mayo de 2018

Warfarin - OMIM - NCBI

Warfarin - OMIM - NCBI

Warfarin

From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.







COUMARIN SENSITIVITY, INCLUDED
Cytogenetic locations: 1pter-p36.13, 19q13.2, 1pter-p36.13, 16p11.2
2.
CHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED
5.
6.
8.
FACTOR V LEIDEN, INCLUDED
Cytogenetic locations: 1q24.2
11.
14.
18.
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