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Q35888853-56040A8A-D21B-4348-ACF4-0FF0018F9221
Q35888853-56040A8A-D21B-4348-ACF4-0FF0018F9221
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http://www.wikidata.org/entity/statement/Q35888853-56040A8A-D21B-4348-ACF4-0FF0018F9221
A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy
P2860
Q35888853-56040A8A-D21B-4348-ACF4-0FF0018F9221
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35888853-56040A8A-D21B-4348-ACF4-0FF0018F9221
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wasDerivedFrom
88a20c09b5b49e9d93f2b6d84bb2a9da3c789278
P2860
Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR.