Mutations in TPM3 are a common cause of congenital fiber type disproportion

Nigel F Clarke; Hannah Kolski; Danielle E Dye; Esther Lim; Robert L L Smith; Rakesh Patel; Michael Collingwood Fahey; Remi Bellance; Norma B Romero; Edward S Johnson; Annick Labarre-Vila; Nicole Monnier; Nigel G Laing; Kathryn N North

doi:10.1002/ana.21308

Mutations in TPM3 are a common cause of congenital fiber type disproportion

Nigel F Clarke, Hannah Kolski, Danielle E Dye, Esther Lim, Robert L L Smith, Rakesh Patel, Michael Collingwood Fahey, Remi Bellance, Norma B Romero, Edward S Johnson, Annick Labarre-Vila, Nicole Monnier, Nigel G Laing, Kathryn N North

Paediatrics Monash Health

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

115 Citations (Scopus)

Original language	English
Pages (from-to)	329 - 337
Number of pages	9
Journal	Annals of Neurology
Volume	63
Issue number	3
DOIs	https://doi.org/10.1002/ana.21308
Publication status	Published - 2008

Access to Document

10.1002/ana.21308

RM sElocation

Cite this

Clarke, Nigel F ; Kolski, Hannah ; Dye, Danielle E ; Lim, Esther ; Smith, Robert L L ; Patel, Rakesh ; Fahey, Michael Collingwood ; Bellance, Remi ; Romero, Norma B ; Johnson, Edward S ; Labarre-Vila, Annick ; Monnier, Nicole ; Laing, Nigel G ; North, Kathryn N. / Mutations in TPM3 are a common cause of congenital fiber type disproportion. In: Annals of Neurology. 2008 ; Vol. 63, No. 3. pp. 329 - 337.

@article{bef092977cd745b5a7cdc67b84efa7b3,

title = "Mutations in TPM3 are a common cause of congenital fiber type disproportion",

author = "Clarke, {Nigel F} and Hannah Kolski and Dye, {Danielle E} and Esther Lim and Smith, {Robert L L} and Rakesh Patel and Fahey, {Michael Collingwood} and Remi Bellance and Romero, {Norma B} and Johnson, {Edward S} and Annick Labarre-Vila and Nicole Monnier and Laing, {Nigel G} and North, {Kathryn N}",

year = "2008",

doi = "10.1002/ana.21308",

language = "English",

volume = "63",

pages = "329 -- 337",

journal = "Annals of Neurology",

issn = "0364-5134",

publisher = "John Wiley & Sons",

number = "3",

}

Mutations in TPM3 are a common cause of congenital fiber type disproportion. / Clarke, Nigel F; Kolski, Hannah; Dye, Danielle E; Lim, Esther; Smith, Robert L L; Patel, Rakesh; Fahey, Michael Collingwood; Bellance, Remi; Romero, Norma B; Johnson, Edward S; Labarre-Vila, Annick; Monnier, Nicole; Laing, Nigel G; North, Kathryn N.

In: Annals of Neurology, Vol. 63, No. 3, 2008, p. 329 - 337.

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

TY - JOUR

T1 - Mutations in TPM3 are a common cause of congenital fiber type disproportion

AU - Clarke, Nigel F

AU - Kolski, Hannah

AU - Dye, Danielle E

AU - Lim, Esther

AU - Smith, Robert L L

AU - Patel, Rakesh

AU - Fahey, Michael Collingwood

AU - Bellance, Remi

AU - Romero, Norma B

AU - Johnson, Edward S

AU - Labarre-Vila, Annick

AU - Monnier, Nicole

AU - Laing, Nigel G

AU - North, Kathryn N

PY - 2008

Y1 - 2008

UR - http://www3.interscience.wiley.com/cgi-bin/fulltext/117922877/PDFSTART

U2 - 10.1002/ana.21308

DO - 10.1002/ana.21308

M3 - Article

VL - 63

SP - 329

EP - 337

JO - Annals of Neurology

JF - Annals of Neurology

SN - 0364-5134

IS - 3

ER -