A novel mutation in the Norrie disease gene.

Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus

Volumn 4, Issue 2, 2000, Pages 125-126

  Ott, S ^a   Patel, R J ^a   Appukuttan, B ^a   Wang, X ^a   Stout, J T ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLINDNESS; CASE REPORT; CHILD; CHROMATOGRAPHY; CODON; GENETICS; HUMAN; MALE; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PROTEIN SYNTHESIS; SYNDROME;

BASE SEQUENCE; BLINDNESS; CHILD; CHROMATOGRAPHY; CODON; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PROTEIN BIOSYNTHESIS; SYNDROME;

EID: 0034166086     PISSN: 10918531     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpa.2000.103874     Document Type: Article

References (0)