Associated Papers
Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka.
Javadiyan S et al.
Molecular Genetics & Genomic Medicine, 2018
Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next-Generation Sequencing.
Ma AS et al.
Human Mutation, 2016
Single-channel SCAM identifies pore-lining residues in the first extracellular loop and first transmembrane domains of Cx46 hemichannels.
Kronengold J et al.
The Journal of General Physiology, 2003
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