Homozygous deletion of the SMN2 gene is a prognostic factor for sporadic amyothrophic lateral sclerosis

J.H. Veldink; L.H. van den Berg; J.M.G. Cobben; R.P. Stulp; V.M.B.P. de Jong; O.J.M. Vogels; F. Baas; J.H.J. Wokke; H Scheffer

Homozygous deletion of the SMN2 gene is a prognostic factor for sporadic amyothrophic lateral sclerosis

Translated title of the contribution: Homozygous deletion of the SMN2 gene is a prognostic factor for sporadic amyothrophic lateral sclerosis

J.H. Veldink, L.H. van den Berg, J.M.G. Cobben, R.P. Stulp, V.M.B.P. de Jong, O.J.M. Vogels, F. Baas, J.H.J. Wokke, H Scheffer

Neurology & Neurosurgery

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

Translated title of the contribution	Homozygous deletion of the SMN2 gene is a prognostic factor for sporadic amyothrophic lateral sclerosis
Original language	Undefined/Unknown
Pages (from-to)	749-752
Number of pages	4
Journal	Neurology
Volume	56
Publication status	Published - 2001

Cite this

@article{f7d0cc7846d14094bef060c407fab019,

title = "Homozygous deletion of the SMN2 gene is a prognostic factor for sporadic amyothrophic lateral sclerosis",

author = "J.H. Veldink and \{van den Berg\}, L.H. and J.M.G. Cobben and R.P. Stulp and \{de Jong\}, V.M.B.P. and O.J.M. Vogels and F. Baas and J.H.J. Wokke and H Scheffer",

year = "2001",

language = "Undefined/Unknown",

volume = "56",

pages = "749--752",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams \& Wilkins",

}

TY - JOUR

T1 - Homozygous deletion of the SMN2 gene is a prognostic factor for sporadic amyothrophic lateral sclerosis

AU - Veldink, J.H.

AU - van den Berg, L.H.

AU - Cobben, J.M.G.

AU - Stulp, R.P.

AU - de Jong, V.M.B.P.

AU - Vogels, O.J.M.

AU - Baas, F.

AU - Wokke, J.H.J.

AU - Scheffer, H

PY - 2001

Y1 - 2001

M3 - Article

SN - 0028-3878

VL - 56

SP - 749

EP - 752

JO - Neurology

JF - Neurology

ER -