Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency

C.A.C. Ottenheijm, C.C. Witt, G.J.M. Stienen, S. Labeit, A.H. Beggs, H. Granzier

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

@article{dd5ea47097a24db18784acb9539f6614,

title = "Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency",

author = "C.A.C. Ottenheijm and C.C. Witt and G.J.M. Stienen and S. Labeit and A.H. Beggs and H. Granzier",

year = "2009",

doi = "10.1093/hmg/ddp168",

language = "Undefined/Unknown",

volume = "18",

pages = "2359--2369",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "13",

}

TY - JOUR

T1 - Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency

AU - Ottenheijm, C.A.C.

AU - Witt, C.C.

AU - Stienen, G.J.M.

AU - Labeit, S.

AU - Beggs, A.H.

AU - Granzier, H.

PY - 2009

Y1 - 2009

U2 - 10.1093/hmg/ddp168

DO - 10.1093/hmg/ddp168

M3 - Article

C2 - 19346529

VL - 18

SP - 2359

EP - 2369

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 13

ER -