Dominant mutations in KBTBD13%25252C a member of the BTB%252…
Dominant mutations in KBTBD13%25252C a member of the BTB%25252FKelch family%25252C cause nemaline myopathy with cores.
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- 1997-06~present; volume:60~present;issue:6~present
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Cell Press
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Coverage:
- 1997-06~present; volume:60~present;issue:6~present
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PubMed Central
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Coverage:
- 1949~6 months ago; volume:1~6 months ago