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Q33843901-50ACAEA1-B9A9-4C89-B13B-098C01666A68
Q33843901-50ACAEA1-B9A9-4C89-B13B-098C01666A68
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Statement
http://www.wikidata.org/entity/statement/Q33843901-50ACAEA1-B9A9-4C89-B13B-098C01666A68
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing
P2860
Q33843901-50ACAEA1-B9A9-4C89-B13B-098C01666A68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33843901-50ACAEA1-B9A9-4C89-B13B-098C01666A68
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wasDerivedFrom
5d1e0ce0cbd70fd1bc6903101f2c5d411087434b
P2860
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy.