A novel mutation in the MAGEL2 gene in a patient with...

Neuromuscular Disorders 2018 / 04 Vol. 28

A novel mutation in the MAGEL2 gene in a patient with arthrogryposis, severe global developmental delay and autistic features

Ardicli, D., Zaharieva, I., Phadke, R., Scoto, M.C., Borrel, L.M., Laurie, S., Agullo, S.B., Sarkozy, A., Muntoni, F.
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Volume:
28
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/S0960-8966(18)30400-0
Date:
April, 2018
File:
PDF, 38 KB
english, 2018
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