๐”– Bobbio Scriptorium
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Clinical and molecular studies of mitochondrial disease

โœ Scribed by Y. Goto


Book ID
110290642
Publisher
Springer
Year
2001
Tongue
English
Weight
141 KB
Volume
24
Category
Article
ISSN
0141-8955

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Mutations in the POLG gene have emerged as one of the most common causes of inherited mitochondrial disease in children and adults. They are responsible for a heterogeneous group of at least 6 major phenotypes of neurodegenerative disease that include: 1) childhood Myocerebrohepatopathy Spectrum dis