Log in to save to my catalogue

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_hal_primary_oai_HAL_hal_03676425v1

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

Muscle contraction upon nerve stimulation relies on excitation–contraction coupling (ECC) to promote the rapid and generalized release of calcium within myofibers. In skeletal muscle, ECC is performed by the direct coupling of a voltage-gated L-type Ca
2+
channel (dihydropyridine receptor; DHPR) located on the T-tubule with a Ca
2+
rele...

Alternative Titles

Full title

Dihydropyridine receptor (DHPR, CACNA1S) congenital myopathy

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_hal_primary_oai_HAL_hal_03676425v1

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_hal_primary_oai_HAL_hal_03676425v1

Other Identifiers

ISSN

0001-6322

E-ISSN

1432-0533

DOI

10.1007/s00401-016-1656-8

How to access this item