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Q36578816-D29A4985-B7AB-4002-BA9F-7D6B79AB7476
Q36578816-D29A4985-B7AB-4002-BA9F-7D6B79AB7476
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Statement
http://www.wikidata.org/entity/statement/Q36578816-D29A4985-B7AB-4002-BA9F-7D6B79AB7476
Common mutations in ALK2/ACVR1, a multi-faceted receptor, have roles in distinct pediatric musculoskeletal and neural orphan disorders.
P2860
Q36578816-D29A4985-B7AB-4002-BA9F-7D6B79AB7476
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36578816-D29A4985-B7AB-4002-BA9F-7D6B79AB7476
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wasDerivedFrom
05e30695b5b00f8ac2d2b38c2785bdb684686e7f
P2860
Alk2 regulates early chondrogenic fate in fibrodysplasia ossificans progressiva heterotopic endochondral ossification