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Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

✍ Scribed by De Sandre-Giovannoli, A


Book ID
127191542
Publisher
BMJ Publishing Group
Year
2003
Tongue
English
Weight
677 KB
Volume
40
Category
Article
ISSN
0022-2593

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