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Q41055576-45868B37-FC0A-4F74-97FB-E70F32CFB07F
Q41055576-45868B37-FC0A-4F74-97FB-E70F32CFB07F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-45868B37-FC0A-4F74-97FB-E70F32CFB07F
Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita.
P2860
Q41055576-45868B37-FC0A-4F74-97FB-E70F32CFB07F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41055576-45868B37-FC0A-4F74-97FB-E70F32CFB07F
rank
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Statement
wasDerivedFrom
e9a1b821c0949e1262fbfa274196431aa7502694
P2860
MutationTaster evaluates disease-causing potential of sequence alterations