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Genet Mol Res ; 15(1)2016 Mar 31.
Article in English | MEDLINE | ID: mdl-27051017

ABSTRACT

The aim of this study was to identify changes in the base sequence of the upstream regulatory region of the transthyretin (TTR) gene. Whole-blood DNA was extracted from ten subjects belonging to a family with familial amyloidosis vitreoretinopathy; the upstream regulatory sequence was amplified by polymerase chain reaction, detected by gel electrophoresis, and sequenced. The DNA sequence of the upstream regulatory region of the TTR gene was successfully sequenced, and a point mutation (-743A→T) was identified in six of the ten blood samples: four patients and two family members without disease incidence. Therefore, a point mutation was identified in the upstream regulatory region of the TTR gene in a Han Chinese family with familial vitreous amyloidosis.


Subject(s)
Amyloidosis, Familial/genetics , Point Mutation/genetics , Prealbumin/genetics , Adolescent , Adult , Exons/genetics , Female , Humans , Male , Middle Aged , Pedigree , Young Adult
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