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Volumn 84, Issue 1, 2013, Pages 91-93

OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHROMOSOME 4Q; CHROMOSOME 4Q24; CHROMOSOME MAP; CLINICAL ARTICLE; FEMALE; GENE; GENE LOCUS; GENETIC LINKAGE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; LETTER; LINKAGE ANALYSIS; MALE; OCULOCUTANEOUS ALBINISM; OCULOCUTANEOUS ALBINISM 5 GENE; PAKISTAN; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SHORT TANDEM REPEAT;

EID: 84879797845     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/cge.12019     Document Type: Letter
Times cited : (85)

References (8)
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    • A review of genetic disorders of hypopigmentation: lessons learned from the biology of melanocytes
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    • ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
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  • 8
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.