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Hereditary spastic paraplegia and peroxisome biogenesis disorders: Case report of a patient with mutations in PEX10 gene
Nascimento, A., Ortez, C., Sariego, A., Gerotina, E., Armstrong, J., Sierra, C., Artuch, R., Jou, C., Jimenez-Mallebrera, C., Colomer, J.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.140
Date:
October, 2015
File:
PDF, 210 KB
english, 2015