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Q27657524-DC8502E1-EC73-474F-BC9B-1E0CD52327B3
Q27657524-DC8502E1-EC73-474F-BC9B-1E0CD52327B3
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http://www.wikidata.org/entity/statement/Q27657524-DC8502E1-EC73-474F-BC9B-1E0CD52327B3
Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders
P2860
Q27657524-DC8502E1-EC73-474F-BC9B-1E0CD52327B3
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Statement
http://www.wikidata.org/entity/statement/Q27657524-DC8502E1-EC73-474F-BC9B-1E0CD52327B3
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63fb96fbb8312a296be9c90efddf9941f0c57e70
P2860
The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy