channel mutation
Recently Published Documents

TOTAL DOCUMENTS

152
(FIVE YEARS 24)

H-INDEX

37
(FIVE YEARS 2)
Latest Documents Most Cited Documents Contributed Authors Related Sources Related Keywords

scholarly journals Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi‐generational family

eJHaem ◽  
2021 ◽  
Author(s):  
Sasha Waldstein ◽  
Sarah Arnold‐Croop ◽  
Laura Carrel ◽  
M. Elaine Eyster
Keyword(s):  
Gardos Channel ◽  
Channel Mutation

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy

2021 ◽  
Author(s):  
Rohan R. Mahale ◽  
Ravindu Tiwari ◽  
Gautham Arunachal ◽  
Hansashree Padmanabha ◽  
Pooja Mailankody
Keyword(s):  
Potassium Channel ◽  
Myoclonic Epilepsy ◽  
Myoclonus Epilepsy ◽  
Progressive Myoclonic Epilepsy ◽  
Channel Mutation

scholarly journals Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Na v 1.7 channel mutation

2020 ◽  
Vol 177 (19) ◽  
pp. 4481-4496 ◽  
Author(s):  
Annika H. Rühlmann ◽  
Jannis Körner ◽  
Ralf Hausmann ◽  
Nikolay Bebrivenski ◽  
Christian Neuhof ◽  
...  
Keyword(s):  
Sodium Channel ◽  
Channel Mutation

Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype

2020 ◽  
Vol 21 (6) ◽  
pp. 932-941 ◽  
Author(s):  
Laure Garcin ◽  
Veronica Mericq ◽  
Anne‐Laure Fauret‐Amsellem ◽  
Helene Cave ◽  
Michel Polak ◽  
...  
Keyword(s):  
Potassium Channel ◽  
Neonatal Diabetes ◽  
Channel Mutation
Load More ...
Sign in / Sign up

Export Citation Format

Share Document