Matches in Nanopublications for { ?s ?p "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191321.RAq5AyrvF-5Z9pyGaOZtjWqpAkgftlsT10va8eZIX9-bY130_provenance.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP277000.RAmJv228mQJWuzRKlZsaAB9BnGdbsNm2DWLgT5s41H3A8130_provenance.
- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_provenance.