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Identification of mutation in PAX9 gene in a Mongolian family with non-syndromic oligodontia / 中华口腔医学杂志
Chinese Journal of Stomatology ; (12): 490-493, 2013.
Article in Chinese | WPRIM | ID: wpr-293575
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the mutation in transcription factor paired box gene PAX9 in a mongolian family with non-syndromic oligodontia.</p><p><b>METHODS</b>Peripheral blood was collected from 17 core family members (9 unaffected, 8 affected) in this Mongolian family with non-syndromic oligodontia. Mutation in exons of PAX9 gene was identified by PCR amplification and DNA sequencing.</p><p><b>RESULTS</b>A point mutation c.87G > C at position 87 in exon 4 of PAX9 was identified from 8 affected members in the family, which were G/C heterozygous.While the 9 healthy members in the family were homozygous for C which was consistent with normal reference sequence in the GenBank(accession number NC_000014).</p><p><b>CONCLUSIONS</b>The mutation of c.87G > C (p. Ala240Pro) in exon 4 of PAX9 was likely to cause the non-syndromic oligodontia in this Mongolian family.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / DNA / Polymerase Chain Reaction / Exons / Sequence Analysis, DNA / Point Mutation / Nucleic Acid Amplification Techniques / Asian People / Ethnology / PAX9 Transcription Factor Type of study: Prognostic study Limits: Adolescent / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Stomatology Year: 2013 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / DNA / Polymerase Chain Reaction / Exons / Sequence Analysis, DNA / Point Mutation / Nucleic Acid Amplification Techniques / Asian People / Ethnology / PAX9 Transcription Factor Type of study: Prognostic study Limits: Adolescent / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Stomatology Year: 2013 Type: Article