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Q33419184-135AFDBB-3A99-437A-BA24-C5A9C2ACC36D
Q33419184-135AFDBB-3A99-437A-BA24-C5A9C2ACC36D
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http://www.wikidata.org/entity/statement/Q33419184-135AFDBB-3A99-437A-BA24-C5A9C2ACC36D
Characterization of 28 novel patients expands the mutational and phenotypic spectrum of Lowe syndrome.
P2860
Q33419184-135AFDBB-3A99-437A-BA24-C5A9C2ACC36D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33419184-135AFDBB-3A99-437A-BA24-C5A9C2ACC36D
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wasDerivedFrom
4fdf0707ab5b9d0b8b8aadee007debd579afcc3d
P2860
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development