Congenital myopathy caused by a novel missense mutation in the CFL2 gene

C.W. Ockeloen; H.J. Gilhuis; R. Pfundt; E.J. Kamsteeg; P.B. Agrawal; A.H. Beggs; A. Dara Hama-Amin; A. Diekstra; N.V.A.M. Knoers; M. Lammens; N. van Alfen

Congenital myopathy caused by a novel missense mutation in the CFL2 gene

Translated title of the contribution: Congenital myopathy caused by a novel missense mutation in the CFL2 gene

C.W. Ockeloen, H.J. Gilhuis, R. Pfundt, E.J. Kamsteeg, P.B. Agrawal, A.H. Beggs, A. Dara Hama-Amin, A. Diekstra, N.V.A.M. Knoers, M. Lammens, N. van Alfen

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

Translated title of the contribution	Congenital myopathy caused by a novel missense mutation in the CFL2 gene
Original language	Undefined/Unknown
Pages (from-to)	632-639
Number of pages	8
Journal	Neuromuscular Disorders
Volume	22
Issue number	7
Publication status	Published - 2012

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/22560515

Cite this

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title = "Congenital myopathy caused by a novel missense mutation in the CFL2 gene",

author = "C.W. Ockeloen and H.J. Gilhuis and R. Pfundt and E.J. Kamsteeg and P.B. Agrawal and A.H. Beggs and {Dara Hama-Amin}, A. and A. Diekstra and N.V.A.M. Knoers and M. Lammens and {van Alfen}, N.",

year = "2012",

language = "Undefined/Unknown",

volume = "22",

pages = "632--639",

journal = "Neuromuscular Disorders",

issn = "0960-8966",

publisher = "Elsevier Limited",

number = "7",

}

TY - JOUR

T1 - Congenital myopathy caused by a novel missense mutation in the CFL2 gene

AU - Ockeloen, C.W.

AU - Gilhuis, H.J.

AU - Pfundt, R.

AU - Kamsteeg, E.J.

AU - Agrawal, P.B.

AU - Beggs, A.H.

AU - Dara Hama-Amin, A.

AU - Diekstra, A.

AU - Knoers, N.V.A.M.

AU - Lammens, M.

AU - van Alfen, N.

PY - 2012

Y1 - 2012

M3 - Article

SN - 0960-8966

VL - 22

SP - 632

EP - 639

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

IS - 7

ER -