z-logo
Premium
A recurrent mutation in the APCDD1 gene responsible for hereditary hypotrichosis simplex in a large Chinese family
Author(s) -
Li M.,
Cheng R.,
Zhuang Y.,
Yao Z.
Publication year - 2012
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2012.11001.x
Subject(s) - medicine , university hospital , family medicine , dermatology , traditional medicine

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here