Mutations of the slow muscle Α-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

D. Wattanasirichaigoon; K.J. Swoboda; F. Takada; H-Q. Tong; V. Lip; S.T. Iannaccone; C. Wallgren-Pettersson; Nigel Laing; A.H. Beggs

Mutations of the slow muscle Α-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

D. Wattanasirichaigoon, K.J. Swoboda, F. Takada, H-Q. Tong, V. Lip, S.T. Iannaccone, C. Wallgren-Pettersson, Nigel Laing, A.H. Beggs

UWA Centre for Medical Research (affiliated with the Harry Perkins Institute of Medical Research)

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

70 Citations (Scopus)

Original language	English
Pages (from-to)	613-617
Journal	Neurology
Volume	59
Publication status	Published - 2002

Cite this

@article{148f6644c57a40baaae202138d1a6fad,

title = "Mutations of the slow muscle Α-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy",

author = "D. Wattanasirichaigoon and K.J. Swoboda and F. Takada and H-Q. Tong and V. Lip and S.T. Iannaccone and C. Wallgren-Pettersson and Nigel Laing and A.H. Beggs",

year = "2002",

language = "English",

volume = "59",

pages = "613--617",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams & Wilkins",

}

TY - JOUR

T1 - Mutations of the slow muscle Α-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy

AU - Wattanasirichaigoon, D.

AU - Swoboda, K.J.

AU - Takada, F.

AU - Tong, H-Q.

AU - Lip, V.

AU - Iannaccone, S.T.

AU - Wallgren-Pettersson, C.

AU - Laing, Nigel

AU - Beggs, A.H.

PY - 2002

Y1 - 2002

M3 - Article

VL - 59

SP - 613

EP - 617

JO - Neurology

JF - Neurology

SN - 0028-3878

ER -