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 paperOther chapter contribution

Original languageEnglish
Title of host publicationHuman Genetics: Diversity and Disease, Monday July 21 to Friday July 25 1997
Place of PublicationPerth
Publication statusPublished - 1997

Cite this

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.