Papers associated with gja8 (and Disease Ontology)

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	Modeling ocular lens disease in Xenopus., Viet J, Reboutier D, Hardy S, Lachke SA, Paillard L, Gautier-Courteille C., Dev Dyn. January 1, 2020; 249 (5): 610-621.
	Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion., Kumari SS, Gandhi J, Mustehsan MH, Eren S, Varadaraj K., Exp Eye Res. November 1, 2013; 116 371-85.
	Mechanism of inhibition of connexin channels by the quinine derivative N-benzylquininium., Rubinos C, Sánchez HA, Verselis VK, Srinivas M., J Gen Physiol. January 1, 2012; 139 (1): 69-82.
	A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts., Arora A, Minogue PJ, Liu X, Addison PK, Russel-Eggitt I, Webster AR, Hunt DM, Ebihara L, Beyer EC, Berthoud VM, Moore AT., J Med Genet. March 1, 2008; 45 (3): 155-60.
	A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract., Arora A, Minogue PJ, Liu X, Reddy MA, Ainsworth JR, Bhattacharya SS, Webster AR, Hunt DM, Ebihara L, Moore AT, Beyer EC, Berthoud VM., J Med Genet. January 1, 2006; 43 (1): e2.
	Molecular mechanism underlying a Cx50-linked congenital cataract., Pal JD, Berthoud VM, Beyer EC, Mackay D, Shiels A, Ebihara L., Am J Physiol. January 1, 1999; 276 (6): C1443-6.

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