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Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism

Authors
Ko, JM; Yang, JA; Jeong, SY; Kim, HJ
Citation
Molecular medicine reports, 5(4):943-948, 2012
Journal Title
Molecular medicine reports
ISSN
1791-29971791-3004
Abstract
Oculocutaneous albinism (OCA) is a group of inherited disorders characterized by defective melanin biosynthesis. OCA1, the most common and severe form, is caused by mutations in the tyrosinase (TYR) gene. OCA4, caused by mutations in the SLC45A2 gene, has frequently been reported in the Japanese population. To determine the mutational spectrum in Korean OCA patients, 12 patients were recruited. The samples were first screened for TYR mutations, and negative samples were screened for SLC45A2 mutations. OCA1 was confirmed in 8 of 12 (66.7%) patients, and OCA4 was diagnosed in 1 (8.3%) patient. In the OCA1 patients, a total of 6 distinct TYR mutations were found in 15 of 16 (93.8%) alleles, all of which had been previously reported. Out of the 6 alleles, c.929insC was the most frequently detected (31.3%), and was mainly associated with OCA1A phenotypes. Other TYR mutations identified included c.1037-7T>A/c.1037-10delTT, p.D383N, p.R77Q and p.R299H. These largely overlapped with mutations found in Japanese and Chinese patients. The SLC45A2 gene analysis identified 1 novel mutation, p.D93N, in 1 patient. This study has provided information on the mutation spectrum in Korean OCA patients, and allows us to estimate the relative frequencies of OCA1 and OCA4 in Korea.
MeSH terms
AdolescentAdultAlbinism, Oculocutaneous/diagnosis/*geneticsAllelesAntigens, Neoplasm/*genetics/metabolismChild, PreschoolExonsFemaleHumansInfantIntronsMaleMembrane Transport Proteins/*genetics/metabolismMonophenol Monooxygenase/*genetics/metabolism*MutationPhenotype
DOI
10.3892/mmr.2012.764
PMID
22294196
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Medical Genetics
AJOU Authors
정, 선용김, 현주
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