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Q34306197-1892BC0D-E7D0-43F3-A3B5-D75C4BD9FA75
Q34306197-1892BC0D-E7D0-43F3-A3B5-D75C4BD9FA75
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http://www.wikidata.org/entity/statement/Q34306197-1892BC0D-E7D0-43F3-A3B5-D75C4BD9FA75
The I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging.
P2860
Q34306197-1892BC0D-E7D0-43F3-A3B5-D75C4BD9FA75
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34306197-1892BC0D-E7D0-43F3-A3B5-D75C4BD9FA75
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wasDerivedFrom
38bbd5848856977d720ea632be0169d741fb075e
P2860
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 gene.