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Q41928481-5A2548BB-491E-4E53-9B5C-A24A56B89A59
Q41928481-5A2548BB-491E-4E53-9B5C-A24A56B89A59
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Statement
http://www.wikidata.org/entity/statement/Q41928481-5A2548BB-491E-4E53-9B5C-A24A56B89A59
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.
P2860
Q41928481-5A2548BB-491E-4E53-9B5C-A24A56B89A59
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41928481-5A2548BB-491E-4E53-9B5C-A24A56B89A59
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wasDerivedFrom
d2c75167dcd80bf27ce1c5126d1b4ec100be42d5
P2860
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).