Results 191 to 194 of about 2,733 (194)

An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutation

Journal of Neurology, Neurosurgery and Psychiatry, 2004
exaly  

0256 Neurophysiological detection of transitory weakness in autosomal recessive myotonia and correlation to CLCN1 gene mutations

Journal of the Neurological Sciences, 2005
openaire   +1 more source

A Novel CLCN1 Gene Mutation Associated with Hypokalemic Periodic Paralysis in a Pregnant Woman.

The Israel Medical Association journal : IMAJ
Jawad, Atrash, Omar, Abu Libdeh, Bashar, Fteiha, Marwan, Abu Sneineh, Alon, Bnaya, Linda, Shavit   +5 more
openaire   +1 more source

Homozygous and Compound Heterozygous Mutations in the CLCN1 Gene Causes Myotonia in Two Related Saudi Families (P2-11.032)

Neurology
Serena Pagliarani, Alwaleed Alabdulwahed, Edoardo Monfrini, Sabrina Lucchiari, Giacomo Comi, Alessio Di Fonzo, Aawadh AlAhmari, Ahmed Abulaban, Wafaa AlEyaid   +8 more
openaire   +1 more source