Homozygous alpha-tropomyosin (TMP3) nonsense mutation in fatal congenital nemaline myopathy

P. Tan, J. Briner, E. Boltshauser, M.R. Davis, Steve Wilton, C. Wallgren-Pettersson, Nigel Laing

Research output: Chapter in Book/Conference paper › Other chapter contribution

Original language	English
Title of host publication	Human Genetics: Diversity and Disease, Monday July 21 to Friday July 25 1997
Place of Publication	Perth
Publication status	Published - 1997

Tan, P., Briner, J., Boltshauser, E., Davis, M. R., Wilton, S., Wallgren-Pettersson, C., & Laing, N. (1997). Homozygous alpha-tropomyosin (TMP3) nonsense mutation in fatal congenital nemaline myopathy. In Human Genetics: Diversity and Disease, Monday July 21 to Friday July 25 1997 Perth.

@inbook{8a706aa55d1d459aac6f0f512c718ecf,

title = "Homozygous alpha-tropomyosin (TMP3) nonsense mutation in fatal congenital nemaline myopathy",

author = "P. Tan and J. Briner and E. Boltshauser and M.R. Davis and Steve Wilton and C. Wallgren-Pettersson and Nigel Laing",

year = "1997",

language = "English",

booktitle = "Human Genetics: Diversity and Disease, Monday July 21 to Friday July 25 1997",

}

Human Genetics: Diversity and Disease, Monday July 21 to Friday July 25 1997. Perth, 1997.

Research output: Chapter in Book/Conference paper › Other chapter contribution

TY - CHAP

T1 - Homozygous alpha-tropomyosin (TMP3) nonsense mutation in fatal congenital nemaline myopathy

AU - Tan, P.

AU - Briner, J.

AU - Boltshauser, E.

AU - Davis, M.R.

AU - Wilton, Steve

AU - Wallgren-Pettersson, C.

AU - Laing, Nigel

PY - 1997

Y1 - 1997

M3 - Other chapter contribution

BT - Human Genetics: Diversity and Disease, Monday July 21 to Friday July 25 1997

CY - Perth

ER -