Matches in Nanopublications for { ?s ?p "[Familial hemiplegic migraine (FHM)-causing mutations in the gene encoding the P/Q Ca(2+) channel alpha(1A) subunit (CACNA1A) locate to the pore and voltage sensor regions and normally involve gain-of-channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_assertion description "[Familial hemiplegic migraine (FHM)-causing mutations in the gene encoding the P/Q Ca(2+) channel alpha(1A) subunit (CACNA1A) locate to the pore and voltage sensor regions and normally involve gain-of-channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787540.RAArw5jpup52vY5UoWgN6_l_CU8XkejdtAsNzmP9I9XxU130_provenance.
- assertion description "[Familial hemiplegic migraine (FHM)-causing mutations in the gene encoding the P/Q Ca(2+) channel alpha(1A) subunit (CACNA1A) locate to the pore and voltage sensor regions and normally involve gain-of-channel function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.