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Molecular Characterization of X-Linked Adrenoleukodystrophy in a Tunisian Family: Identification of a Novel Missense Mutation in the ABCD1 Gene
Kallabi, Fakhri, Hadj Salem, Ikhlass, Ben Salah, Ghada, Ben Turkia, Hadhami, Ben Chehida, Amel, Tebib, Neji, Fakhfakh, Faiza, Kamoun, HassenVolume:
12
Year:
2013
Language:
english
Journal:
Neurodegenerative Diseases
DOI:
10.1159/000346680
File:
PDF, 405 KB
english, 2013