Novel mutations in FRMD7 in X-linked congenital nystagmus. Mutation in brief #963. Online.

Human mutation

Volumn 28, Issue 5, 2007, Pages 525-

  Schorderet, Daniel F ^a   Tiab, Leila ^a   Gaillard, Marie Claire ^a   Lorenz, Birgit ^a   Klainguti, Georges ^a   Kerrison, John B ^a   Traboulsi, Elias I ^a   Munier, Francis L ^a  

^a Institut de Recherche en Ophtalmologie   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSKELETON PROTEIN; FRMD7 PROTEIN, HUMAN; MEMBRANE PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME MAP; CONGENITAL NYSTAGMUS; GENETICS; HUMAN; MUTATION; X CHROMOSOME LINKED DISORDER;

CHROMOSOME MAPPING; CYTOSKELETAL PROTEINS; GENETIC DISEASES, X-LINKED; HUMANS; MEMBRANE PROTEINS; MUTATION; NYSTAGMUS, CONGENITAL;

EID: 34250643196     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9492     Document Type: Article

References (0)