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Q30396131-9B3D1D83-A05E-4EE3-86DA-FB623446019A
Q30396131-9B3D1D83-A05E-4EE3-86DA-FB623446019A
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http://www.wikidata.org/entity/statement/Q30396131-9B3D1D83-A05E-4EE3-86DA-FB623446019A
SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations.
P2860
Q30396131-9B3D1D83-A05E-4EE3-86DA-FB623446019A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30396131-9B3D1D83-A05E-4EE3-86DA-FB623446019A
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wasDerivedFrom
7c008c74f4bf585ad276ab3afac6b125856c7fa4
P2860
Congenital hereditary endothelial dystrophy caused by SLC4A11 mutations progresses to Harboyan syndrome.