A mutation in the a tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

Nigel Laing; Steve Wilton; P.A. Akkari; S. Dorosz; K. Boundy; C. Kneebone; P. Blumbergs; S. White; H. Watkins; D.R. Love; E. Haan

A mutation in the a tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

Nigel Laing
, Steve Wilton
, P.A. Akkari
, S. Dorosz
, K. Boundy
, C. Kneebone
, P. Blumbergs
, S. White
, H. Watkins
, D.R. Love
, E. Haan

UWA Centre for Medical Research (affiliated with the Harry Perkins Institute of Medical Research)
Centre for Neuromuscular and Neurological Disorders (Perron Institute)

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

60 Citations (Web of Science)

Original language	English
Pages (from-to)	75-79
Journal	Nature Genetics
Volume	9
Issue number	January
Publication status	Published - 1995

Cite this

@article{31bcd31c52c144c0a0c70cd91ed56b4a,

title = "A mutation in the a tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy",

author = "Nigel Laing and Steve Wilton and P.A. Akkari and S. Dorosz and K. Boundy and C. Kneebone and P. Blumbergs and S. White and H. Watkins and D.R. Love and E. Haan",

year = "1995",

language = "English",

volume = "9",

pages = "75--79",

journal = "Nature Genetics",

publisher = "Nature Research",

number = "January",

}

TY - JOUR

T1 - A mutation in the a tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

AU - Laing, Nigel

AU - Wilton, Steve

AU - Akkari, P.A.

AU - Dorosz, S.

AU - Boundy, K.

AU - Kneebone, C.

AU - Blumbergs, P.

AU - White, S.

AU - Watkins, H.

AU - Love, D.R.

AU - Haan, E.

PY - 1995

Y1 - 1995

M3 - Article

VL - 9

SP - 75

EP - 79

JO - Nature Genetics

JF - Nature Genetics

IS - January

ER -