Exome sequencing reveals a novel Moroccan founder mutation...

Brain 2013 / 03 Vol. 136; Iss. 3

Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome

Gerards, M., Kamps, R., van Oevelen, J., Boesten, I., Jongen, E., de Koning, B., Scholte, H. R., de Angst, I., Schoonderwoerd, K., Sefiani, A., Ratbi, I., Coppieters, W., Karim, L., de Coo, R., van de
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Volume:
136
Language:
english
Journal:
Brain
DOI:
10.1093/brain/awt013
Date:
March, 2013
File:
PDF, 551 KB
english, 2013
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