Homo sapiens calcium channel, voltage-dependent, alpha 2/delta subunit - Nucleotide

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A New Zebrafish Model for CACNA2D4-Dysfunction. [Invest Ophthalmol Vis Sci. 2019]
A New Zebrafish Model for CACNA2D4-Dysfunction.
Schlegel DK, Glasauer SMK, Mateos JM, Barmettler G, Ziegler U, Neuhauss SCF. Invest Ophthalmol Vis Sci. 2019 Dec 2; 60(15):5124-5135.
Founder Ashkenazi Jewish mutations of large deletion in the inherited retinal dystrophy genes. [Ophthalmic Genet. 2018]
Founder Ashkenazi Jewish mutations of large deletion in the inherited retinal dystrophy genes.
Chiang JP, Luo H, Duan J, Ekstein J, Hirsch Y. Ophthalmic Genet. 2018 Jan-Feb; 39(1):135-136. Epub 2017 Jul 20.
Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans. [Ophthalmology. 2016]
Mutations in CACNA2D4 Cause Distinctive Retinal Dysfunction in Humans.
Ba-Abbad R, Arno G, Carss K, Stirrups K, Penkett CJ, Moore AT, Michaelides M, Raymond FL, Webster AR, Holder GE. Ophthalmology. 2016 Mar; 123(3):668-71.e2. Epub 2015 Nov 7.

RefSeq alternative splicing
See 13 reference mRNA sequence splice variants for the CACNA2D4 gene.

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Nucleotide