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Analysis of PCCA and PCCB gene mutations in patients with propionic acidemia / 中华医学遗传学杂志
Article in Zh | WPRIM | ID: wpr-239542
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To analyze PCCA and PCCB gene mutations in 10 Chinese patients with propionic acidemia(PA).</p><p><b>METHODS</b>Genomic DNA was extracted from peripheral blood leukocytes. The 39 exons and flanking sequences of the PCCA and PCCB genes were amplified with polymerase chain reaction and subjected to direct DNA sequencing.</p><p><b>RESULTS</b>DNA sequencing has revealed that 7 patients have carried a PCCA gene mutation, 2 patients carried PCCB gene mutation and 1 patient carried mutations in both PCCA and PCCB genes. Ten PA mutations were confirmed, including 8 affecting the PCCA gene and 2 affecting the PCCB gene. Three PCCA mutations c.245G>A, IVS15+5del5, c.1288C>T and 2 PCCB mutations c.838insC, c.1087T>C were found for the first time.</p><p><b>CONCLUSION</b>Among Chinese patients with propionic acidemia patients, their genetic mutations are mainly found on the PCCA gene.</p>
Subject(s)
Full text: 1 Database: WPRIM Main subject: Methylmalonyl-CoA Decarboxylase / Propionic Acidemia / Genetics / Mutation Limits: Child, preschool / Female / Humans / Infant / Male Language: Zh Journal: Chinese Journal of Medical Genetics Year: 2015 Document type: Article
Full text: 1 Database: WPRIM Main subject: Methylmalonyl-CoA Decarboxylase / Propionic Acidemia / Genetics / Mutation Limits: Child, preschool / Female / Humans / Infant / Male Language: Zh Journal: Chinese Journal of Medical Genetics Year: 2015 Document type: Article
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