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Mechanisms of disease and clinical features of mutations of the gene for mitofusin 2: an important cause of hereditary peripheral neuropathy with striking clinical variability in children and adults

✍ Scribed by ROBERT OUVRIER; SIMON GREW


Book ID
111131415
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
134 KB
Volume
52
Category
Article
ISSN
0012-1622

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