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1-29-04 Double trouble: A3243G point mutation in the mitochondrial DNA in a patient homozygous for the most common nonsense mutation of amp deaminase gene

✍ Scribed by Y. Campos; J.C. Rubio; M.A. Martín; J. Bautista; J. Arenas


Book ID
119469078
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
178 KB
Volume
150
Category
Article
ISSN
0022-510X

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