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Q36993758-64A81CAB-CED8-4A1F-A0CA-DD727F611C99
Q36993758-64A81CAB-CED8-4A1F-A0CA-DD727F611C99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36993758-64A81CAB-CED8-4A1F-A0CA-DD727F611C99
A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
P2860
Q36993758-64A81CAB-CED8-4A1F-A0CA-DD727F611C99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36993758-64A81CAB-CED8-4A1F-A0CA-DD727F611C99
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type
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Statement
wasDerivedFrom
12b77a4bb071d863ef45acf1542af2565dc6e94a
P2860
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma