Characterization of the NPHP1 locus: Mutational mechanism involved in deletions in familial juvenile nephronophthisis

American Journal of Human Genetics

Volumn 66, Issue 3, 2000, Pages 778-789

  Saunier, Sophie ^a   Calado, Joaquim ^a   Benessy, France ^a   Silbermann, Flora ^a   Heilig, Roland ^b   Weissenbach, Jean ^b   Antignac, Corinne ^a,c  

^a INSERM   (France)

^b CENTRE NATIONAL DE SÉQUENÇAGE   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 2Q; CHROMOSOME BREAKAGE; CHROMOSOME REARRANGEMENT; CHRONIC KIDNEY FAILURE; CLINICAL ARTICLE; CROSSING OVER; GENE DELETION; GENE LOCUS; GENE MAPPING; GENETIC RECOMBINATION; HUMAN; NEPHRONOPHTHISIS; PRIORITY JOURNAL;

EID: 0033941864     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302819     Document Type: Article

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