An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental Jews

Human Genetics

Volumn 128, Issue 3, 2010, Pages 261-267

  Zelinger, Lina ^a   Greenberg, Alex ^a   Kohl, Susanne ^b   Banin, Eyal ^a   Sharon, Dror ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AGE; ARTICLE; AUTOSOMAL INHERITANCE; CENTROMERE; CHROMOSOME 2; CHROMOSOME ANALYSIS; COLOR BLINDNESS; GENE FLOW; GENE MUTATION; GENOME; GENOME ANALYSIS; GENOMICS; GENOTYPE; HAPLOTYPE; HUMAN; INFORMATION PROCESSING; JEW; MICROANALYSIS; MIDDLE EAST; MOSLEM; POPULATION; PRIORITY JOURNAL; RING CHROMOSOME; SINGLE NUCLEOTIDE POLYMORPHISM; Y CHROMOSOME; ALLELE; ARAB; COLOR VISION DEFECT; CONSANGUINITY; FOUNDER EFFECT; GENE FREQUENCY; GENETICS; HOMOZYGOTE; ISLAM; ISRAEL; POINT MUTATION; TIME;

ALLELES; ARABS; COLOR VISION DEFECTS; CONSANGUINITY; CYCLIC NUCLEOTIDE-GATED CATION CHANNELS; FOUNDER EFFECT; GENE FREQUENCY; HAPLOTYPES; HOMOZYGOTE; HUMANS; ISLAM; ISRAEL; JEWS; MIDDLE EAST; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; TIME FACTORS;

CNGA3 PROTEIN, HUMAN; CYCLIC NUCLEOTIDE GATED CHANNEL;

EID: 77956058284     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-010-0846-z     Document Type: Article

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