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The axonal form of autosomal recessive Charcot-Marie-Tooth (CMT) disease: a phenotype study of 4 Moroccan families

✍ Scribed by N. Birouk; H. Belaidi; A. Benomar; A. Bouhouche; B. Kably; R. Ouazzani; M. Yahyaoui; E. Le Guern; T. Chkili

Book ID: 117670883
Publisher: Elsevier Science
Year: 1997
Tongue: English
Weight: 130 KB
Volume: 7
Category: Article
ISSN: 0960-8966
DOI: 10.1016/s0960-8966(97)87335-x

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