Publication | Open Access
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract
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Citations
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References
2012
Year
Impaired TraffickingMip/aqp0 MutationOcular DiseaseDevelopmental BiologyFunction UnderliesOphthalmologyGenetic DisorderGeneticsMolecular GeneticsMedicine
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