Different functional outcome of RetGC1 and RPE65 gene mutations in leber congenital amaurosis [5]

American Journal of Human Genetics

Volumn 64, Issue 4, 1999, Pages 1225-1228

  Perrault, I ^a   Rozet, J M ^a   Ghazi, I ^a   Leowski, C ^a   Bonnemaison, M ^a   Gerber, S ^a   Ducroq, D ^a   Cabot, A ^a   Souied, E ^a   Dufier, J L ^a   Munnich, A ^a   Kaplan, J ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CONSANGUINEOUS MARRIAGE; GENE MAPPING; GENE MUTATION; LEBER CONGENITAL AMAUROSIS; LETTER; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA DYSTROPHY; SEGREGATION ANALYSIS; TREATMENT OUTCOME;

EID: 0033362015     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302335     Document Type: Letter

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