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Q41979823-3DE757E8-40FE-4C8A-B9E9-769857724802
Q41979823-3DE757E8-40FE-4C8A-B9E9-769857724802
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41979823-3DE757E8-40FE-4C8A-B9E9-769857724802
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities
P2860
Q41979823-3DE757E8-40FE-4C8A-B9E9-769857724802
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41979823-3DE757E8-40FE-4C8A-B9E9-769857724802
rank
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Statement
wasDerivedFrom
78b833d4b54aa74521d4609a892b29dd98855cf7
P2860
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene