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MeSH:(Myotonia Congenita*)

3.Phenotypic Difference of CLCN1 Gene Variant (A313T) in a Korean Family with Myotonia Congenita.

Jin Sung PARK ; Sun Jae HWANG ; Jin Hong SHIN

Journal of the Korean Neurological Association 2016;34(3):220-223

4.Two Cases of Becker's Type Congenital Myotonia.

In Soo MOON ; Dae Soo JUNG ; Kyu Hyun PARK

Journal of the Korean Neurological Association 1996;14(2):605-611

5.A Case of Becker's Type Congenital Myotonia.

Sung Hwan YUN ; Jung Sang HAH ; Jun LEE

Yeungnam University Journal of Medicine 1999;16(1):125-130

6.Myotonia Dystrophica: A Case Report

Joon Young KIM ; Young Joe KIM ; Byeong Yeon SEONG ; Moon Ho HWANG

The Journal of the Korean Orthopaedic Association 1985;20(1):195-199

7.Clinical Characteristics and Analysis of CLCN1 in Patients with "EMG Disease".

Tai Seung NAM ; Hyun Jung JUNG ; Seok Yong CHOI ; Young Ok KIM ; Myeong Kyu KIM ; Ki Hyun CHO

Journal of Clinical Neurology 2012;8(3):212-217

8.Analysis of CLCN1 gene mutations in 2 patients with myotonia congenita.

Zhi-ting CHEN ; Jin HE ; Wan-jin CHEN ; Sheng-gen CHEN ; Ji-lan LIN ; Qin-yong YE ; Hua-pin HUANG

Chinese Journal of Medical Genetics 2012;29(6):690-692

10.Electrophysiological characteristics of R47W and A298T mutations in CLC-1 of myotonia congenita patients and evaluation of clinical features.

Hyung Jin CHIN ; Chan Hyeong KIM ; Kotdaji HA ; Jin Hong SHIN ; Dae Seong KIM ; Insuk SO

The Korean Journal of Physiology and Pharmacology 2017;21(4):439-447

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