A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21

Human Molecular Genetics

Volumn 6, Issue 1, 1997, Pages 27-31

  Chaïb, Hassan ^a   Kaplan, Josseline ^b   Gerber, Sylvie ^b   Vincent, Christophe ^a   Ayadi, Hammadi ^c   Slim, Rima ^d   Munnich, Arnold ^b   Weissenbach, Jean ^e   Petit, Christine ^a  

^a CNRS   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c UNIVERSITY OF SFAX   (Tunisia)

^d AMERICAN UNIVERSITY OF BEIRUT   (Lebanon)

^e GÉNÉTHON   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 21Q; CHROMOSOME MAP; CLINICAL ARTICLE; CONGENITAL DEAFNESS; GENE LOCUS; HOMOZYGOSITY; HUMAN; MOROCCO; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; USHER SYNDROME;

EID: 0031032971     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.1.27     Document Type: Article

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