TY  - GEN
AU  - Baig,Shahid M
AU  - Koschak,Alexandra
AU  - Lieb,Andreas
AU  - Gebhart,Mathias
AU  - Dafinger,Claudia
AU  - Nürnberg,Gudrun
AU  - Ali,Amjad
AU  - Ahmad,Ilyas
AU  - Sinnegger-Brauns,Martina J
AU  - Brandt,Niels
AU  - Engel,Jutta
AU  - Mangoni,Matteo E
AU  - Farooq,Muhammad
AU  - Khan,Habib U
AU  - Nürnberg,Peter
AU  - Striessnig,Jörg
AU  - Bolz,Hanno J
TI  - Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness
SN  - 1546-1726
PY  - 2011///0203
KW  - Adolescent
KW  - Adult
KW  - Bradycardia
KW  - genetics
KW  - Calcium Channels, L-Type
KW  - Channelopathies
KW  - Deafness
KW  - congenital
KW  - Female
KW  - HEK293 Cells
KW  - Hair Cells, Auditory, Inner
KW  - physiology
KW  - Haplotypes
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Protein Isoforms
KW  - Sinoatrial Node
KW  - Syndrome
KW  - Transfection
KW  - methods
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1038/nn.2694
ER  -