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Q43707344-B74890B1-13A1-49B3-B273-DE34E063D60F
Q43707344-B74890B1-13A1-49B3-B273-DE34E063D60F
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Statement
http://www.wikidata.org/entity/statement/Q43707344-B74890B1-13A1-49B3-B273-DE34E063D60F
A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2.
P2860
Q43707344-B74890B1-13A1-49B3-B273-DE34E063D60F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43707344-B74890B1-13A1-49B3-B273-DE34E063D60F
rank
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type
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Statement
wasDerivedFrom
bf33265c5046e2f4ac269652cd8cfb3bea678c8d
P2860
Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects