Mutations in human lipoyltransferase gene LIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase - Concepedia

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Mutations in human lipoyltransferase gene LIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase

DOI Full Paper Access

100

Citations

16

References

2013

Year

Yohan Sorèze, Audrey Boutron, Florence Habarou, Christine Barnérias, Luc Nonnenmacher, Hélène Delpech, Asmaa Mamoune, Dominique Chrétien, Laurence Hubert, Christine Bôle‐Feysot,

Orphanet Journal of Rare Diseases

References

	Year	Citations

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