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Compound mutations ofPEO1andTYMPin a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype

✍ Scribed by Khriezhanuo Nakhro; Ki Wha Chung; Seung-Min Kim; Il-Nam Sunwoo; Eun Min Cho; Sun Wha Park; Jung Hee Hwang; Byung-Ok Choi


Book ID
107693635
Publisher
The Genetics Society of Korea
Year
2011
Tongue
English
Weight
384 KB
Volume
33
Category
Article
ISSN
1976-9571

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