199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

Anne T Bertrand; Carsten G Bonnemann; Gisele Bonne; Christina Anne Mitchell; Meagan Jane Mcgrath

doi:10.1016/j.nmd.2014.02.002

199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

Anne T Bertrand, Carsten G Bonnemann, Gisele Bonne, Christina Anne Mitchell, Meagan Jane Mcgrath

Biochemistry & Molecular Biology

Research output: Contribution to journal › Article › Other

7 Citations (Scopus)

Original language	English
Pages (from-to)	453 - 462
Number of pages	10
Journal	Neuromuscular Disorders
Volume	24
Issue number	5
DOIs	https://doi.org/10.1016/j.nmd.2014.02.002
Publication status	Published - 2014

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10.1016/j.nmd.2014.02.002

2428782-oaFinal published version, 617 KB

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title = "199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands",

author = "Bertrand, {Anne T} and Bonnemann, {Carsten G} and Gisele Bonne and Mitchell, {Christina Anne} and Mcgrath, {Meagan Jane}",

year = "2014",

doi = "10.1016/j.nmd.2014.02.002",

language = "English",

volume = "24",

pages = "453 -- 462",

journal = "Neuromuscular Disorders",

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publisher = "Elsevier",

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T1 - 199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

AU - Bertrand, Anne T

AU - Bonnemann, Carsten G

AU - Bonne, Gisele

AU - Mitchell, Christina Anne

AU - Mcgrath, Meagan Jane

PY - 2014

Y1 - 2014

UR - http://www.ncbi.nlm.nih.gov/pubmed/24613424

U2 - 10.1016/j.nmd.2014.02.002

DO - 10.1016/j.nmd.2014.02.002

M3 - Article

VL - 24

SP - 453

EP - 462

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

SN - 0960-8966

IS - 5

ER -

199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

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Identification of the molecular mechanisms by which mutations in FHL1 lead to protein misfolding and skeletal muscle disease

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199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

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Identification of the molecular mechanisms by which mutations in FHL1 lead to protein misfolding and skeletal muscle disease

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