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Q47911970-3EF76D6C-1B11-43B0-BDBB-8439E2788FCB
Q47911970-3EF76D6C-1B11-43B0-BDBB-8439E2788FCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47911970-3EF76D6C-1B11-43B0-BDBB-8439E2788FCB
A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.
P2860
Q47911970-3EF76D6C-1B11-43B0-BDBB-8439E2788FCB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47911970-3EF76D6C-1B11-43B0-BDBB-8439E2788FCB
rank
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Statement
wasDerivedFrom
852334134191dc0d2b5f2c006d42729037fa7675
P2860
Blau syndrome-associated Nod2 mutation alters expression of full-length NOD2 and limits responses to muramyl dipeptide in knock-in mice.