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  An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract
 
 
Title: An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract
Author: Senthil Kumar, G.
Kyle, John W.
Minogue, Peter J.
Dinesh Kumar, K.
Vasantha, K.
Berthoud, Viviana M.
Beyer, Eric C.
Santhiya, S.T.
Appeared in: Experimental eye research
Paging: Volume 110 (2013) nr. C pages 6 p.
Year: 2013
Contents:
Publisher: Elsevier Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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