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Q34425375-94FB7B86-7EC9-464D-BEBE-948C01EE1EDB
Q34425375-94FB7B86-7EC9-464D-BEBE-948C01EE1EDB
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http://www.wikidata.org/entity/statement/Q34425375-94FB7B86-7EC9-464D-BEBE-948C01EE1EDB
Novel mutations in PXDN cause microphthalmia and anterior segment dysgenesis.
P2860
Q34425375-94FB7B86-7EC9-464D-BEBE-948C01EE1EDB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34425375-94FB7B86-7EC9-464D-BEBE-948C01EE1EDB
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3764181a9cd38f848b5db7e420c27299ea2e4b5e
P2860
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.