Mutational screening of peripherine/RDS, rhodopsine and ROM-1 genes in 69 index patients with retinitis pigmentosa and allied retinal dystrophies;Depistage mutationnel des genes de la peripherine/RDS, rhodopsine et ROM-1 dans 69 cas index de retinite pigmentaire et autres dystrophies retiniennes

Klinische Monatsblatter fur Augenheilkunde

Volumn 212, Issue 5, 1998, Pages 305-308

  Milla E ^a   Heon E ^b   Piguet, B ^a   Ducrey, N ^a   Butler, N ^c   Stone, E ^d   Schorderet, D F ^d   Munier, F ^a  

^a HÔPITAL OPHTALMIQUE JULES GONIN   (Switzerland)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

^d UNIVERSITY OF LAUSANNE   (Switzerland)

Author keywords

Autosomal dominant inheritance; Macular dystrophy; Peripherin RDS; Retinitis pigmentosa; Rhodopsin

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; GENE MUTATION; GENE SEGREGATION; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; MAJOR CLINICAL STUDY; PHENOTYPE; RETINA MACULA DEGENERATION; RETINITIS PIGMENTOSA; SEQUENCE ANALYSIS;

EID: 0031841684     PISSN: 00232165     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1034890     Document Type: Article

References (20)

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