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Q39438083-0C6D57E2-A668-48AD-AEFD-0A1A3E203FB8
Q39438083-0C6D57E2-A668-48AD-AEFD-0A1A3E203FB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39438083-0C6D57E2-A668-48AD-AEFD-0A1A3E203FB8
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
P2860
Q39438083-0C6D57E2-A668-48AD-AEFD-0A1A3E203FB8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39438083-0C6D57E2-A668-48AD-AEFD-0A1A3E203FB8
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Statement
wasDerivedFrom
1ce6e192057a5af4d95b60f20f7c03e2e0832a92
P2860
CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder