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Q45061895-6BFFB1EE-6AA0-46B6-BF0A-3F7E5A210C92
Q45061895-6BFFB1EE-6AA0-46B6-BF0A-3F7E5A210C92
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http://www.wikidata.org/entity/statement/Q45061895-6BFFB1EE-6AA0-46B6-BF0A-3F7E5A210C92
C-terminal truncated dystrophin identified in skeletal muscle of an asymptomatic boy with a novel nonsense mutation of the dystrophin gene.
P2860
Q45061895-6BFFB1EE-6AA0-46B6-BF0A-3F7E5A210C92
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45061895-6BFFB1EE-6AA0-46B6-BF0A-3F7E5A210C92
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wasDerivedFrom
895bda8da894d40f933d0a9f9905399bec088538
P2860
Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.