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P54 A dominant negative mutation in FBXO38 is a cause of distal hereditary motor neuropathy (dHMN)

✍ Scribed by Rossor, A.M.; d'Ydewalle, C.; Wooley, J.; Harms, M.; Reilly, M.M.; Greensmith, L.; Sumner, C.; Houlden, H.

Book ID: 122693586
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 56 KB
Volume: 24
Category: Article
ISSN: 0960-8966
DOI: 10.1016/S0960-8966(14)70070-7

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