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Q34015436-2F8BE358-DC30-453E-8B5A-F1B66D896D98
Q34015436-2F8BE358-DC30-453E-8B5A-F1B66D896D98
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http://www.wikidata.org/entity/statement/Q34015436-2F8BE358-DC30-453E-8B5A-F1B66D896D98
A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.
P2860
Q34015436-2F8BE358-DC30-453E-8B5A-F1B66D896D98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34015436-2F8BE358-DC30-453E-8B5A-F1B66D896D98
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wasDerivedFrom
2da8ac8c86b75bfec923e539c2ad195e9b52a842
P2860
Structural basis for vertebrate filamin dimerization.