Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathy

Biochemical and Biophysical Research Communications

Volumn 246, Issue 1, 1998, Pages 35-38

  Shastry, Barkur S ^a  

^a OAKLAND UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONTROLLED STUDY; EXUDATE; FEMALE; GENETIC ANALYSIS; GENETIC COUNSELING; HUMAN; HUMAN CELL; INFANT; MALE; MISSENSE MUTATION; NORRIE DISEASE; PRESCHOOL CHILD; PRIORITY JOURNAL; VITREORETINOPATHY;

EID: 0032495997     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1998.8565     Document Type: Article

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