NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect

F Baertling; L Sanchez-Caballero; MAM van den Brand; C W Fung; SHS Chan; V C N Wong; DME Hellebrekers; IFM Coo; JAM Smeitink; RJT Rodenburg; LGJ Nijtmans

doi:10.1111/cge.13089

NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect

F Baertling, L Sanchez-Caballero, MAM van den Brand, C W Fung, SHS Chan, V C N Wong, DME Hellebrekers, IFM Coo, JAM Smeitink, RJT Rodenburg, LGJ Nijtmans

Neurology

Research output: Contribution to journal › Article › Academic › peer-review

37 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	111-118
Number of pages	8
Journal	Clinical Genetics
Volume	93
Issue number	1
DOIs	https://doi.org/10.1111/cge.13089
Publication status	Published - 2018

Research programs

EMC OR-01

Access to Document

10.1111/cge.13089

http://hdl.handle.net/1765/103031

Cite this

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title = "NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect",

author = "F Baertling and L Sanchez-Caballero and {van den Brand}, MAM and Fung, {C W} and SHS Chan and Wong, {V C N} and DME Hellebrekers and IFM Coo and JAM Smeitink and RJT Rodenburg and LGJ Nijtmans",

year = "2018",

doi = "10.1111/cge.13089",

language = "Undefined/Unknown",

volume = "93",

pages = "111--118",

journal = "Clinical Genetics",

issn = "0009-9163",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "1",

}

TY - JOUR

T1 - NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect

AU - Baertling, F

AU - Sanchez-Caballero, L

AU - van den Brand, MAM

AU - Fung, C W

AU - Chan, SHS

AU - Wong, V C N

AU - Hellebrekers, DME

AU - Coo, IFM

AU - Smeitink, JAM

AU - Rodenburg, RJT

AU - Nijtmans, LGJ

PY - 2018

Y1 - 2018

U2 - 10.1111/cge.13089

DO - 10.1111/cge.13089

M3 - Article

C2 - 28671271

SN - 0009-9163

VL - 93

SP - 111

EP - 118

JO - Clinical Genetics

JF - Clinical Genetics

IS - 1

ER -