Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families.

Human mutation

Volumn 15, Issue 4, 2000, Pages 388-

  Adato, A ^a   Weston, M D ^a   Berry, A ^a   Kimberling, W J ^a   Bonne Tamir, A ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

SCLEROPROTEIN; USH2A PROTEIN, HUMAN;

ADOLESCENT; ADULT; ARTICLE; CONSANGUINITY; FEMALE; GENETIC POLYMORPHISM; GENETICS; HEARING IMPAIRMENT; HETEROZYGOSITY LOSS; HUMAN; ISRAEL; MALE; MIDDLE AGED; MUTATION; PRESCHOOL CHILD; RETINITIS PIGMENTOSA; SYNDROME;

ADOLESCENT; ADULT; CHILD, PRESCHOOL; CONSANGUINITY; DEAFNESS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; HUMANS; ISRAEL; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, GENETIC; RETINITIS PIGMENTOSA; SYNDROME;

EID: 0034164449     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(200004)15:4<388::AID-HUMU27>3.0.CO;2-N     Document Type: Article

References (0)