Matches in Nanopublications for { ?s ?p "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566902.RAnBcFsjHdszUyUjBLiPoLvifikeVV6Y0gCMN_1QA-OA8130_provenance.
- NP806878.RAlC7O0dz6i2ipyT700ANGorfehdtvfmeMKRDBQuWvVYc130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806878.RAlC7O0dz6i2ipyT700ANGorfehdtvfmeMKRDBQuWvVYc130_provenance.
- NP507014.RAyU5zBru67BOXoYeXXfF_8AFfh1ajQr_YqHyACsET55k130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507014.RAyU5zBru67BOXoYeXXfF_8AFfh1ajQr_YqHyACsET55k130_provenance.
- NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539982.RAIa-hwImODb5er0z-RdHZG0v2DAY0VvoSM_eaWQiCtag130_provenance.
- NP358920.RABwTwBRbne0hBMqwzQctpX2Ha4UnMgjbiyyw79maJvhk130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358920.RABwTwBRbne0hBMqwzQctpX2Ha4UnMgjbiyyw79maJvhk130_provenance.
- NP359097.RAqHx0nqg3XfRDHM72d_zFg_dvWwZm76nTVrByxqczgmQ130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP359097.RAqHx0nqg3XfRDHM72d_zFg_dvWwZm76nTVrByxqczgmQ130_provenance.
- NP1316522.RAcbo0RXPvDhVOorp3jB7HTYqiqQv7tvSy1XZTQtkXtu8130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316522.RAcbo0RXPvDhVOorp3jB7HTYqiqQv7tvSy1XZTQtkXtu8130_provenance.
- NP1316524.RAUtOUMBR1dCHRIO8-SlYD59rVECjUHwGmH5vN6qTNQEM130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316524.RAUtOUMBR1dCHRIO8-SlYD59rVECjUHwGmH5vN6qTNQEM130_provenance.
- NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225911.RArFgRa0eafMkDFv0DwXUivODOJ9ZYBm6l3FLBWhDam-Y130_provenance.
- NP1316525.RAh12cI2XIQJdp74ER0ulxzvUOgOWMmiB3VPVPSVer8cQ130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316525.RAh12cI2XIQJdp74ER0ulxzvUOgOWMmiB3VPVPSVer8cQ130_provenance.
- NP225742.RA5BlOn7q115INOFqSGSNScclgfNFuS8MFhGc29Nf83mk130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225742.RA5BlOn7q115INOFqSGSNScclgfNFuS8MFhGc29Nf83mk130_provenance.
- NP1316521.RA00cSgQWVQfpp0GMdl-l_cQs4y-9Zly8_TcZMigKG2-4130_assertion description "[Mutations in the gene encoding the alpha 1-subunit of the skeletal muscle dihydropyridine (DHP) receptor are responsible for familial hypokalaemic periodic paralysis (HypoPP), an autosomal dominant muscle disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1316521.RA00cSgQWVQfpp0GMdl-l_cQs4y-9Zly8_TcZMigKG2-4130_provenance.