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Q30833220-C3815C49-C811-4563-B197-D1D5C5E7338E
Q30833220-C3815C49-C811-4563-B197-D1D5C5E7338E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30833220-C3815C49-C811-4563-B197-D1D5C5E7338E
Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy.
P921
Q30833220-C3815C49-C811-4563-B197-D1D5C5E7338E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30833220-C3815C49-C811-4563-B197-D1D5C5E7338E
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type
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Statement
P921
birth defect