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

✍ Scribed by Dubourg, O.; Birouk, N.; Bouhouche, A.; Azzedine, H.; Benomar, A.; Belaïdi, H.; Muriel, M.P.; Maisonobe, T.; Yahyaoui, M.; Le Guern, E.

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