Biallelic mutations in Oxa1l cause a mitochondrial...

Neuromuscular Disorders 2018 / 04 Vol. 28

Biallelic mutations in Oxa1l cause a mitochondrial encephalopathy and combined oxidative phosphorylation dysfunction

Thompson, K., Mai, N., Olahova, M., Scialo, F., Formosa, L.E., Stroud, D.A., Garett, M., Lax, N.Z., Jou, C., Nascimento, A., Ortez, C., Jimenez-Mallabrera, C., Hardy, S.A., He, L., Brown, G.K., Martti
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Volume:
28
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/s0960-8966(18)30392-4
Date:
April, 2018
File:
PDF, 19 KB
english, 2018
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