Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease

MJ Blok, L Spruijt, IFM Coo, Kees Schoonderwoerd, A Hendrickx, HJ Smeets

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@article{cb62002f4ff244888e479d88ff413561,

title = "Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease",

author = "MJ Blok and L Spruijt and IFM Coo and Kees Schoonderwoerd and A Hendrickx and HJ Smeets",

year = "2007",

language = "Undefined/Unknown",

volume = "44",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "4",

}

TY - JOUR

T1 - Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease

AU - Blok, MJ

AU - Spruijt, L

AU - Coo, IFM

AU - Schoonderwoerd, Kees

AU - Hendrickx, A

AU - Smeets, HJ

PY - 2007

Y1 - 2007

M3 - Article

SN - 0022-2593

VL - 44

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 4

ER -