Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

R Brugnoni, E Canioni, M Filosto, A Pini, P Tonin… - neurogenetics - Springer
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …
被引用次数：12 相关文章

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

R Brugnoni, E Canioni, M Filosto, A Pini, P Tonin… - …, 2021 - iris.unibs.it
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

R Brugnoni, E Canioni, M Filosto, A Pini, P Tonin… - …, 2021 - air.unimi.it
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

R Brugnoni, E Canioni, M Filosto, A Pini… - …, 2022 - pubmed.ncbi.nlm.nih.gov
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …

[引用][C] Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

R Brugnoni, E Canioni, M Filosto, A Pini, P Tonin… - neurogenetics, 2021 - cir.nii.ac.jp
Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete
analysis of CACNA1S and SCN4A genes | CiNii Research CiNii 国立情報学研究所 学術情報 …

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

B Raffaella, C Eleonora, F Massimiliano… - …, 2022 - search.proquest.com
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes.

R Brugnoni, E Canioni, M Filosto, A Pini, P Tonin… - Neurogenetics, 2021 - europepmc.org
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …

Mutations associated with hypokalemic periodic paralysis: from hotspot regions to complete analysis of CACNA1S and SCN4A genes

R Brugnoni, E Canioni, M Filosto, A Pini, P Tonin… - NEUROGENETICS, 2022 - iris.univr.it
Familial periodic paralyses (PPs) are inherited disorders of skeletal muscle characterized by
recurrent episodes of flaccid muscle weakness. PPs are classified as hypokalemic …