Dominant mutations in KBTBD13%2525252C a member of the BTB%2…
Dominant mutations in KBTBD13%2525252C a member of the BTB%2525252FKelch family%2525252C cause nemaline myopathy with cores.
Article, Chapter
Full text availability for this item
Collection:
Elsevier ScienceDirect Journals
Coverage:
- 1997-06~present
Collection:
Cell Press
Coverage:
- 1997-06~present
Collection:
PubMed Central
Coverage:
- 1949~6 months ago