Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

Nature Genetics

Volumn 18, Issue 1, 1998, Pages 11-12

  Martínez Mir, Amalia ^a   Paloma, Eva ^a   Allikmets, Rando ^b   Ayuso, Carmen ^c   Del Río, Teresa ^c   Dean, Michael ^d   Vilageliu, Lluïsa ^a   Gonzàlez Duarte, Roser ^a   Balcells, Susana ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b SAIC FREDERICK INC   (United States)

^c Clínica Nuestra Señora de la Concepción   (Spain)

^d NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABCA4 PROTEIN, HUMAN;

FEMALE; FRAMESHIFT MUTATION; GENETICS; HOMOZYGOTE; HUMAN; MALE; NOTE; PEDIGREE; RECESSIVE GENE; RETINA MACULA DEGENERATION; RETINITIS PIGMENTOSA;

ATP-BINDING CASSETTE TRANSPORTERS; FEMALE; FRAMESHIFT MUTATION; GENES, RECESSIVE; HOMOZYGOTE; HUMANS; MACULAR DEGENERATION; MALE; PEDIGREE; RETINITIS PIGMENTOSA;

EID: 0031606609     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0198-11     Document Type: Article

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