GJA3
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- Genome-Wide Gene Expression Profiling of Randall's Plaques In
- Original Article Targeted Exome Sequencing Identified a Novel GJA3 Gene Missense Mutation Causes Autosomal Dominant Congenital Cataract in a Large Chinese Family
- Reduced Penetrance in Human Inherited Disease
- Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
- Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging
- Whole Exome Sequencing Reveals Novel and Recurrent Disease‐Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract
- Mechanisms of Cellular Metabolic Regulation in Short-Term Hypoxia
- Microarray Analysis of Iris Gene Expression in Mice with Mutations Influencing Pigmentation
- A Novel Mutation in the GJA3 (Connexin46) Gene Is Associated with Autosomal Dominant Congenital Nuclear Cataract in a Chinese Family
- A Novel Missense Mutation in the Gene for Gap-Junction Protein α3 (GJA3) Associated with Autosomal Dominant •Œnuclear Pu
- Signal Transduction Pathway Products
- A Biphasic Role for the Voltage-Gated Sodium Channel Scn5lab
- Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
- Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease
- Plasma Membrane Protein Identifications from Human Bone Marrow Mesenchymal Stem Cells
- Supplement Table S2
- Somatic Mutations
- Gap Junction Channelopathies and Calmodulinopathies. Do Disease-Causing Calmodulin Mutants Affect Direct Cell–Cell Communication?