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Co-existing point mutations of mitochondrial DNA in a patient with a heart abnormality and Pearson syndrome-like symptoms

✍ Scribed by Kae Munakata; Miki Bundo; Tadafumi Kato; Hiroaki Ono; Nobuo Sakura; Minoru Oosaki; Chiaki Waki; Masashi Tanaka


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
147 KB
Volume
139A
Category
Article
ISSN
1552-4825

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