Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand

Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand

Leber hereditary optic neuropathy (LHON) is the most common mitochondrially inherited disease causing blindness, preferentially in young adult males. Most of the patients carry the G11778A mitochondrial DNA (mtDNA) mutation. However, the marked incomplete penetrance and the gender bias indicate some...

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Main Authors: Nopasak Phasukkijwatana, Bussaraporn Kunhapan, Jim Stankovich, Wanicha L. Chuenkongkaew, Russell Thomson, Timothy Thornton, Melanie Bahlo, Taisei Mushiroda, Yusuke Nakamura, Surakameth Mahasirimongkol, Aung Win Tun, Chatchawan Srisawat, Chanin Limwongse, Chayanon Peerapittayamongkol, Thanyachai Sura, Wichit Suthammarak, Patcharee Lertrit
Other Authors: Mahidol University
Format: Article
Published: 2018
Subjects:
Biochemistry, Genetics and Molecular Biology
Medicine
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/28683
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Institution: Mahidol University

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https://repository.li.mahidol.ac.th/handle/123456789/28683

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