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Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 23(4): 1161-4, 2015 Aug.
Artigo em Chinês | MEDLINE | ID: mdl-26314465

RESUMO

OBJECTIVE: To identify the mutation of ENG and ALK1 genes in a hereditary hemorrhagic telangiectasia pedigree. METHODS: 14 exons of ENG gene and 9 exons of ALK1 gene in 11 menbers of this pedigree 4 generation were amplified by reverse transcription-polymerase chain reaction (RT-PCR), the PCR products were screened by direct sequencing. RESULTS: A nonsense mutation c.447G > A was found in exon 4 of ENG gen of the pedigreee, resulting in change of Trp 149 into Stop, while no gene mutation was found in ALK1 gene. CONCLUSION: The hereditary hemorrhagic telangiectasia in this pedigree is caused by the nonsense mutation c.447G > A in ENG gene.


Assuntos
Telangiectasia Hemorrágica Hereditária , Códon sem Sentido , Éxons , Humanos , Mutação , Linhagem , Reação em Cadeia da Polimerase
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