Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

S. Herdewyn; H. Zhao; M. Moisse; V. Race; G. Matthijs; J. Reumers; B. Kusters; H.J. Schelhaas; L.H. van den Berg; A. Goris; W. Robberecht; D. Lambrechts; P. van Damme

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

Translated title of the contribution: Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

S. Herdewyn
, H. Zhao
, M. Moisse
, V. Race
, G. Matthijs
, J. Reumers
, B. Kusters
, H.J. Schelhaas
, L.H. van den Berg
, A. Goris
, W. Robberecht
, D. Lambrechts
, P. van Damme

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

Translated title of the contribution	Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis
Original language	Undefined/Unknown
Pages (from-to)	2412-2419
Number of pages	8
Journal	Human Molecular Genetics
Volume	21
Issue number	11
Publication status	Published - 2012

Keywords

Econometric and Statistical Methods: General
Geneeskunde(GENK)
Medical sciences
Bescherming en bevordering van de menselijke gezondheid

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/22343411

Cite this

Herdewyn, S., Zhao, H., Moisse, M., Race, V., Matthijs, G., Reumers, J., Kusters, B., Schelhaas, H. J., van den Berg, L. H., Goris, A., Robberecht, W., Lambrechts, D., & van Damme, P. (2012). Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis. Human Molecular Genetics, 21(11), 2412-2419. http://www.ncbi.nlm.nih.gov/pubmed/22343411

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title = "Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis",

keywords = "Econometric and Statistical Methods: General, Geneeskunde(GENK), Medical sciences, Bescherming en bevordering van de menselijke gezondheid",

author = "S. Herdewyn and H. Zhao and M. Moisse and V. Race and G. Matthijs and J. Reumers and B. Kusters and H.J. Schelhaas and \{van den Berg\}, L.H. and A. Goris and W. Robberecht and D. Lambrechts and \{van Damme\}, P.",

year = "2012",

language = "Undefined/Unknown",

volume = "21",

pages = "2412--2419",

journal = "Human Molecular Genetics",

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Herdewyn, S, Zhao, H, Moisse, M, Race, V, Matthijs, G, Reumers, J, Kusters, B, Schelhaas, HJ, van den Berg, LH, Goris, A, Robberecht, W, Lambrechts, D & van Damme, P 2012, 'Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis', Human Molecular Genetics, vol. 21, no. 11, pp. 2412-2419. <http://www.ncbi.nlm.nih.gov/pubmed/22343411>

Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis. / Herdewyn, S.; Zhao, H.; Moisse, M. et al.
In: Human Molecular Genetics, Vol. 21, No. 11, 2012, p. 2412-2419.

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

TY - JOUR

T1 - Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis

AU - Herdewyn, S.

AU - Zhao, H.

AU - Moisse, M.

AU - Race, V.

AU - Matthijs, G.

AU - Reumers, J.

AU - Kusters, B.

AU - Schelhaas, H.J.

AU - van den Berg, L.H.

AU - Goris, A.

AU - Robberecht, W.

AU - Lambrechts, D.

AU - van Damme, P.

PY - 2012

Y1 - 2012

KW - Econometric and Statistical Methods: General

KW - Geneeskunde(GENK)

KW - Medical sciences

KW - Bescherming en bevordering van de menselijke gezondheid

M3 - Article

SN - 0964-6906

VL - 21

SP - 2412

EP - 2419

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 11

ER -