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Mutations in human lipoyltransferase geneLIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase
Yohan Soreze,Audrey Boutron,Florence Habarou…Volume:
8
Langue:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/1750-1172-8-192
Date:
December, 2013
Fichier:
PDF, 1008 KB
english, 2013