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Q34306197-ACF8027F-0287-4BF3-9169-D7CDD8A43CB1
Q34306197-ACF8027F-0287-4BF3-9169-D7CDD8A43CB1
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http://www.wikidata.org/entity/statement/Q34306197-ACF8027F-0287-4BF3-9169-D7CDD8A43CB1
The I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging.
P2860
Q34306197-ACF8027F-0287-4BF3-9169-D7CDD8A43CB1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34306197-ACF8027F-0287-4BF3-9169-D7CDD8A43CB1
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wasDerivedFrom
37c4aad6c26ce3105bf5a23e2e85ce5014306c3c
P2860
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor.