A NOVEL MUTATION (C201R) IN THE TRANSMEMBRANE DOMAIN OF CONNEXIN-32 IN SEVERE X-LINKED CHARCOT-MARIE-TOOTH DISEASE

Authors
SILLEN A ANNEREN G DAHL N
Citation
A. Sillen et al., A NOVEL MUTATION (C201R) IN THE TRANSMEMBRANE DOMAIN OF CONNEXIN-32 IN SEVERE X-LINKED CHARCOT-MARIE-TOOTH DISEASE, Human mutation, 1998, pp. 8-9
Citations number
11
Categorie Soggetti
Genetics & Heredity
Journal title
Human mutation → ACNP
ISSN journal
10597794
Year of publication
1998
Supplement
1
Pages
8 - 9
Database
ISI
SICI code
1059-7794(1998):<8:ANM(IT>2.0.ZU;2-R