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Q41845181-A22C0316-A036-41FF-B044-C59170D14991
Q41845181-A22C0316-A036-41FF-B044-C59170D14991
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Statement
http://www.wikidata.org/entity/statement/Q41845181-A22C0316-A036-41FF-B044-C59170D14991
Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophy.
P2860
Q41845181-A22C0316-A036-41FF-B044-C59170D14991
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41845181-A22C0316-A036-41FF-B044-C59170D14991
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wasDerivedFrom
ee45d688ead123a7d94b9307455e7b47feb032b0
P2860
Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.