THE TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM LOCUS MAPS TO CHROMOSOME 15Q11.2-Q12

被引:0
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作者
RAMSAY, M
COLMAN, MA
STEVENS, G
ZWANE, E
KROMBERG, J
FARRALL, M
JENKINS, T
机构
[1] S AFRICAN INST MED RES,SCH PATHOL,DEPT HUMAN GENET,MRC,HUMAN ECOGENET RES UNIT,JOHANNESBURG 2000,SOUTH AFRICA
[2] UNIV WITWATERSRAND,JOHANNESBURG 2001,SOUTH AFRICA
[3] NORTHWICK PK HOSP & CLIN RES CTR,CLIN RES CTR,DIV MOLEC MED,HARROW HA1 3UJ,MIDDX,ENGLAND
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中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Tyrosinase-positive oculocutaneous albinism (ty-pos OCA), an autosomal recessive disorder of the melanin biosynthetic pathway, is the most common type of albinism occurring worldwide. In southern African Bantu-speaking negroids it has an overall prevalence of about 1/3,900. Since the basic biochemical defect is unknown, a linkage study with candidate loci, candidate chromosomal regions, and random loci was undertaken. The ty-pos OCA locus was found to be linked to two arbitrary loci, D15S10 and D15S13, in the Prader-Willi/Angelman chromosomal region on chromosome 15q11.2-q12. The pink-eyed dilute locus, p, on mouse chromosome 7, maps close to a region of homology on human chromosome 15q, and we postulate that the ty-pos OCA and p loci are homologous.
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页码:879 / 884
页数:6
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