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De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring

✍ Scribed by Már H. Tulinius; Massoud Houshmand; Nils-Göran Larsson; Elisabeth Holme; Anders Oldfors; Eva Holmberg; Jan Wahlström


Book ID
104666036
Publisher
Springer
Year
1995
Tongue
English
Weight
434 KB
Volume
96
Category
Article
ISSN
0340-6717

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