|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.