R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?

Authors
Lopez-Bigas, N Rabionet, R Arbones, ML Estivill, X
Citation
N. Lopez-bigas et al., R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?, EUR J HUM G, 9(1), 2001, pp. 70-70
Citations number
3
Categorie Soggetti
Molecular Biology & Genetics
Journal title
EUROPEAN JOURNAL OF HUMAN GENETICS
ISSN journal
10184813 → ACNP
Volume
9
Issue
1
Year of publication
2001
Pages
70 - 70
Database
ISI
SICI code
1018-4813(200101)9:1<70:RVIC3M>2.0.ZU;2-3