P.17.11 c.250G>A in ETFDH, a common sequence variant in...

Neuromuscular Disorders 2013 / 10 Vol. 23; Iss. 9-10

P.17.11 c.250G>A in ETFDH, a common sequence variant in southern Chinese population is a pathogenic mutation to cause multiple acyl-CoA dehydrogenase deficiency

Liang, W.C., Lin, Y.F., Liu, D.Y., Nishino, I., Jong, Y.J.
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.661
Date:
October, 2013
File:
PDF, 50 KB
english, 2013
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