Null mutations causing depletion of the type 1 ryanodine rec…
Null mutations causing depletion of the type 1 ryanodine receptor %25252528RYR1%25252529 are commonly associated with recessive structural congenital myopathies with cores.
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Journal:
Human MutationOpens in new Window
Collection:
Wiley Online Library Database Model 2021
Coverage:
- 1996~present
Journal:
Human MutationOpens in new Window
Collection:
Wiley Online Library: Complete Journals
Coverage:
- 1996-01-01~2022-12-01