Source:http://linkedlifedata.com/resource/pubmed/id/11499668
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2001-8-13
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pubmed:abstractText |
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a heterogeneous enzyme abnormality with high frequency in tropical areas. We performed population screening and molecular studies of G6PD variants to clarify their distribution and features in Southeast Asia. A total of 4317 participants (2019 males, 2298 females) from 16 ethnic groups in Myanmar, Lao in Laos, and Amboinese in Indonesia were screened with a single-step screening method. The prevalence of G6PD-deficient males ranged from 0% (the Akha) to 10.8% (the Shan). These G6PD-deficient individuals and 12 G6PD-deficient patients who had been diagnosed at hospitals in Indonesia and Malaysia were subjected to molecular analysis by a combination of polymerase-chain-reaction-based single-strand conformation polymorphism analysis and direct sequencing. Ten different missense mutations were identified in 63 G6PD-deficient individuals (50 hemizygotes, 11 heterozygotes, and 2 homozygotes) from 14 ethnic groups. One missense mutation (1291 G-->A) found in an Indonesian Chinese, viz., G6PD Surabaya, was previously unknown. The 487 G-->A (G6PD Mahidol) mutation was widely seen in Myanmar, 383 T-->C (G6PD Vanua Lava) was specifically found among Amboinese, 871 G-->A (G6PD Viangchan) was observed mainly in Lao, and 592 C-->T (G6PD Coimbra) was found in Malaysian aborigines (Orang Asli). The other five mutations, 95 A-->G (G6PD Gaohe), 1003 G-->A (G6PD Chatham), 1360 C-->T (G6PD Union), 1376 G-->T (G6PD Canton), and 1388 G-->A (G6PD Kaiping) were identified mostly in accordance with distributions reported previously.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0340-6717
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pubmed:author |
pubmed-author:DachlanY PYP,
pubmed-author:FujiiHH,
pubmed-author:HidayahN INI,
pubmed-author:HironoAA,
pubmed-author:HorieTT,
pubmed-author:IshiiAA,
pubmed-author:IwaiKK,
pubmed-author:KawamotoFF,
pubmed-author:LinKK,
pubmed-author:MatsuokaHH,
pubmed-author:MiwaSS,
pubmed-author:NotopuroHH,
pubmed-author:SalimA MAM,
pubmed-author:TantularI SIS
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pubmed:issnType |
Print
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pubmed:volume |
108
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
445-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11499668-Amino Acid Substitution,
pubmed-meshheading:11499668-Asia, Southeastern,
pubmed-meshheading:11499668-DNA,
pubmed-meshheading:11499668-DNA Mutational Analysis,
pubmed-meshheading:11499668-Female,
pubmed-meshheading:11499668-Genetic Testing,
pubmed-meshheading:11499668-Geography,
pubmed-meshheading:11499668-Glucosephosphate Dehydrogenase,
pubmed-meshheading:11499668-Glucosephosphate Dehydrogenase Deficiency,
pubmed-meshheading:11499668-Humans,
pubmed-meshheading:11499668-Male,
pubmed-meshheading:11499668-Mutation,
pubmed-meshheading:11499668-Point Mutation
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pubmed:year |
2001
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pubmed:articleTitle |
Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia.
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pubmed:affiliation |
Department of Medical Zoology, Jichi Medical School, Tochigi, Japan. kuni@jichi.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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