TY  - GEN
AU  - Mustapha,Mirna
AU  - Chouery,Eliane
AU  - Torchard-Pagnez,Delphine
AU  - Nouaille,Sylvie
AU  - Khrais,Awni
AU  - Sayegh,Fouad N
AU  - Mégarbané,André
AU  - Loiselet,Jacques
AU  - Lathrop,Mark
AU  - Petit,Christine
AU  - Weil,Dominique
TI  - A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25
SN  - 0340-6717
PY  - 2002///0621
KW  - Adult
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 17
KW  - Female
KW  - Genetic Linkage
KW  - Hearing Loss, Sensorineural
KW  - genetics
KW  - Humans
KW  - Male
KW  - Pedigree
KW  - Retinitis Pigmentosa
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s00439-002-0690-x
ER  -