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A novel mutation in theABCD1gene of a Moroccan patient with X-linked adrenoleukodystrophy: case report
Karkar, Adnane, Barakat, Abdelhamid, Bakhchane, Amina, Fettah, Houda, Slassi, Ilham, Dorboz, Imen, Boespflug-Tanguy, Odile, Nadifi, SellamaVolume:
15
Language:
english
Journal:
BMC Neurology
DOI:
10.1186/s12883-015-0503-1
Date:
December, 2015
File:
PDF, 778 KB
english, 2015