TY  - GEN
AU  - Ye,Dan
AU  - Tester,David J
AU  - Zhou,Wei
AU  - Papagiannis,John
AU  - Ackerman,Michael J
TI  - A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel
SN  - 1556-3871
PY  - 2020///1002
KW  - Adolescent
KW  - Autism Spectrum Disorder
KW  - genetics
KW  - Bradycardia
KW  - diagnosis
KW  - Calcium Channels, L-Type
KW  - Cells, Cultured
KW  - DNA
KW  - DNA Mutational Analysis
KW  - Electrocardiography
KW  - Humans
KW  - Male
KW  - Mutation, Missense
KW  - Patch-Clamp Techniques
KW  - Pedigree
KW  - Romano-Ward Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.hrthm.2018.08.030
ER  -