Phenotypical features of 11 Moroccan families with autosomal recessive Charcot-Marie-tooth disease associated with mutations in the gdap1 gene

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Bibliographic Details
Published in:Revue neurologique 2007-04, Vol.163 (4), p.489-490
Main Authors: Birouk, N., Bouhouche, A., Azzedine, H., Dubourg, O., Benomar, A., Belaïdi, H., Muriel, M.P., Maisonobe, T., Yahyaoui, M., Le Guern, E., Ouazzani, R.
Format: Article
Language:fre
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ISSN:0035-3787
DOI:10.1016/S0035-3787(07)90444-0