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The expanding phenotype of hypokalemic periodic paralysis i..:
Kurokawa, Mari
;
Torio, Michiko
;
Ohkubo, Kazuhiro
...
Molecular Genetics & Genomic Medicine. 8 (2020) 4 - p. , 2020
Link:
https://doi.org/10.1002/mgg3.1175
RT Journal T1
The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_mgg3.1175&Exemplar=1&LAN=DE A1 Kurokawa, Mari A1 Torio, Michiko A1 Ohkubo, Kazuhiro A1 Tocan, Vlad A1 Ohyama, Noriko A1 Toda, Naoko A1 Ishii, Kanako A1 Nishiyama, Kei A1 Mushimoto, Yuichi A1 Sakamoto, Ryuichi A1 Nakaza, Maki A1 Horie, Riho A1 Kubota, Tomoya A1 Takahashi, Masanori P. A1 Sakai, Yasunari A1 Nomura, Masatoshi A1 Ohga, Shouichi PB Wiley YR 2020 SN 2324-9269 SN 2324-9269 JF Molecular Genetics & Genomic Medicine VO 8 IS 4 LK http://dx.doi.org/https://doi.org/10.1002/mgg3.1175 DO https://doi.org/10.1002/mgg3.1175 SF ELIB - SuUB Bremen
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