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- Title
Familial hemiplegic migraine mutations affect P/Q-Type Ca<sup>2+</sup> channel gating.
- Abstract
The article presents an abstract of the report "Familial hemiplegic migraine mutations affect P/Q-Type Ca2+ channel gating." Familial Hemiplegic Migraine (FHM) is an autosomal dominant neurological disorder associated with missense mutations. It was found out that FHM mutations, like the previously reported mutations T666M, V714A, and I1819L, affect P/Q-type Ca2+ channel gating.
- Subjects
MIGRAINE; GENETIC mutation; ANIMAL mutation; HEMIPLEGICS
- Publication
Pflügers Archiv: European Journal of Physiology, 2000, Vol 439, pR330
- ISSN
0031-6768
- Publication type
Abstract