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Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNAphe gene

✍ Scribed by N. Darin; G. Kollberg; A-R. Moslemi; M. Tulinius; E. Holme; M. Andersson Grönlund; S. Andersson; A. Oldfors


Book ID
116792468
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
192 KB
Volume
16
Category
Article
ISSN
0960-8966

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