Molecular diagnosis of an unconventional 5'splice site mutation causing congenital liver fibrosis

Normally, disease-causing 5′ splice-site (5′ss) mutations disrupt Watson-Crick/wobble base pair(s) with U1 small nuclear RNA (snRNA) but some mutations do not. In this thesis, we investigated a T→C mutation in hemochromatosis (HFE) intron 2 which might break a possible non-canonical Ψ-U base pair in...

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書目詳細資料
主要作者: Muhammad Ridhwan Mohammad Muzaki
其他作者: Xavier Roca Castella
格式: Final Year Project
語言:English
出版: 2016
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在線閱讀:http://hdl.handle.net/10356/67360
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