AIFM1 mutation presenting with fatal...

Molecular Case Studies 2017 / 03 Vol. 3; Iss. 2

AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant

Morton, Sarah U., Prabhu, Sanjay P., Lidov, Hart G.W., Shi, Jiahai, Anselm, Irina, Brownstein, Catherine A., Bainbridge, Matthew N., Beggs, Alan H., Vargas, Sara O., Agrawal, Pankaj B.
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Volume:
3
Language:
english
Journal:
Molecular Case Studies
DOI:
10.1101/mcs.a001560
Date:
March, 2017
File:
PDF, 2.79 MB
english, 2017
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