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Q52602020-090CC77C-DB43-4F19-891D-8FCE3A1D9BBD
Q52602020-090CC77C-DB43-4F19-891D-8FCE3A1D9BBD
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Statement
http://www.wikidata.org/entity/statement/Q52602020-090CC77C-DB43-4F19-891D-8FCE3A1D9BBD
Skeletal, cardiac, and respiratory muscle function and histopathology in the P448Lneo- mouse model of FKRP-deficient muscular dystrophy.
P2860
Q52602020-090CC77C-DB43-4F19-891D-8FCE3A1D9BBD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52602020-090CC77C-DB43-4F19-891D-8FCE3A1D9BBD
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type
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wasDerivedFrom
c0c3617e268cc0be62999f9d20f26e2c234c1428
P2860
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.