Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.

AH Hakonen; S Goffart; S Marjavaara; A Paetau; Helen Cooper; K Mattila; M Lampinen; A Sajantila; T Lönnqvist; JN Spelbrink; A. Suomalainen

doi:10.1093/hmg/ddn280

Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.

AH Hakonen, S Goffart, S Marjavaara, A Paetau, Helen Cooper, K Mattila, M Lampinen, A Sajantila, T Lönnqvist, JN Spelbrink, A. Suomalainen

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122 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	3822–3835
Journal	Human Molecular Genetics
Volume	17
Issue number	23
DOIs	https://doi.org/10.1093/hmg/ddn280
Publication status	Published - 2008
MoE publication type	A1 Journal article-refereed

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10.1093/hmg/ddn280

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Hakonen, AH., Goffart, S., Marjavaara, S., Paetau, A., Cooper, H., Mattila, K., Lampinen, M., Sajantila, A., Lönnqvist, T., Spelbrink, JN., & Suomalainen, A. (2008). Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion. Human Molecular Genetics, 17(23), 3822–3835. https://doi.org/10.1093/hmg/ddn280

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title = "Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.",

author = "AH Hakonen and S Goffart and S Marjavaara and A Paetau and Helen Cooper and K Mattila and M Lampinen and A Sajantila and T L{\"o}nnqvist and JN Spelbrink and A. Suomalainen",

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Hakonen, AH, Goffart, S, Marjavaara, S, Paetau, A, Cooper, H, Mattila, K, Lampinen, M, Sajantila, A, Lönnqvist, T, Spelbrink, JN & Suomalainen, A 2008, 'Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.', Human Molecular Genetics, vol. 17, no. 23, pp. 3822–3835. https://doi.org/10.1093/hmg/ddn280

TY - JOUR

T1 - Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion.

AU - Hakonen, AH

AU - Goffart, S

AU - Marjavaara, S

AU - Paetau, A

AU - Cooper, Helen

AU - Mattila, K

AU - Lampinen, M

AU - Sajantila, A

AU - Lönnqvist, T

AU - Spelbrink, JN

AU - Suomalainen, A.

PY - 2008

Y1 - 2008

U2 - 10.1093/hmg/ddn280

DO - 10.1093/hmg/ddn280

M3 - Artikel

SN - 0964-6906

VL - 17

SP - 3822

EP - 3835

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 23

ER -