A new mutation in MT-ND1 m.3928G>C p.V208L causes Leigh disease with infantile spasms-Reference-Cited by-同舟云学术

A new mutation in MT-ND1 m.3928G>C p.V208L causes Leigh disease with infantile spasms

Published:2013-11 Issue:6 Volume:13 Page:656-661
ISSN:1567-7249
Container-title:Mitochondrion
language:en
Short-container-title:Mitochondrion

Author:

Wray Carter D.,Friederich Marisa W.,du Sart Desiree,Pantaleo Sarah,Smet Joél,Kucera Cathlin,Fenton Laura,Scharer Gunter,Van Coster Rudy,Van Hove Johan L.K.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

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4. Energy converting NADH:quinone oxidoreductase (complex I);Brandt;Annu. Rev. Biochem.,2006

5. Bilateral striatal necrosis and MELAS associated with a new T3308C mutation in the mitochondrial ND1 gene;Campos;Biochem. Biophys. Res. Commun.,1997

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