MYOSIN-VIIA, THE GENE-PRODUCT DEFECTIVE IN THE DEAF BLINDNESS DISEASEUSHER SYNDROME TYPE 1B, EXHIBITS A UNIQUE EXPRESSION PROFILE IN COCHLEA AND RETINA

Authors
HASSON T HEINTZELMAN MB SANTOSSACCHI J COREY DP MOOSEKER MS
Citation
T. Hasson et al., MYOSIN-VIIA, THE GENE-PRODUCT DEFECTIVE IN THE DEAF BLINDNESS DISEASEUSHER SYNDROME TYPE 1B, EXHIBITS A UNIQUE EXPRESSION PROFILE IN COCHLEA AND RETINA, Molecular biology of the cell, 6, 1995, pp. 836-836
Citations number
NO
Categorie Soggetti
Cell Biology",Biology
Journal title
Molecular biology of the cell → ACNP
ISSN journal
10591524
Volume
6
Year of publication
1995
Supplement
S
Pages
836 - 836
Database
ISI
SICI code
1059-1524(1995)6:<836:MTGDIT>2.0.ZU;2-K