Matches in Nanopublications for { ?s ?p "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP247864.RAjwzdlvxFkouRjJ6JjOgUqjTpywq6EEUm8lN-TR4PIr0130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP247864.RAjwzdlvxFkouRjJ6JjOgUqjTpywq6EEUm8lN-TR4PIr0130_provenance.
- NP287716.RAvsqd88hNSy2m0mKpNSCSp6B1Ym1eoerPySjRKim_hOA130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP287716.RAvsqd88hNSy2m0mKpNSCSp6B1Ym1eoerPySjRKim_hOA130_provenance.
- assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP277160.RADUKFCXMAk-wLctFXTUewcfPvY_BWiBYnyD5AlXuZnMY130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277160.RADUKFCXMAk-wLctFXTUewcfPvY_BWiBYnyD5AlXuZnMY130_provenance.
- NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717655.RAtQorUhtXyW_1ojN4ZLuUznq_XxOaUgyA2FVS_vLR-q0130_provenance.
- NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277182.RA-nk6LmG9BkKQdEzg0rKwRxDPvitHbZU9KGVKBBFlCkI130_provenance.
- NP717656.RA4gVEeWDrq7Y9-X4yLPJxll-_XAHtIrQckiBGwS0sivg130_assertion description "[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717656.RA4gVEeWDrq7Y9-X4yLPJxll-_XAHtIrQckiBGwS0sivg130_provenance.