A Novel Mutation in CLCN1 Associated with Feline Myotonia Congenita

Truncating CLCN1 mutations in myotonia congenita: Variable patterns of inheritance

(2013) Randal C. Richardson et al.   MUSCLE & NERVE

Clinical and molecular study of a new form of hereditary myotonia in Murrah water buffalo

(2013) Alexandre S. Borges et al.   NEUROMUSCULAR DISORDERS

Widespread recognition of 5' splice sites by noncanonical base-pairing to U1 snRNA involving bulged nucleotides

(2012) X. Roca et al.   GENES & DEVELOPMENT

First WNK4-Hypokalemia Animal Model Identified by Genome-Wide Association in Burmese Cats

(2012) Barbara Gandolfi et al.   PLoS One

A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony

(2011) Inge D. Wijnberg et al.   NEUROMUSCULAR DISORDERS

New insights into RNA secondary structure in the alternative splicing of pre-mRNAs

(2011) Yongfeng Jin et al.   RNA Biology

Structure of a Eukaryotic CLC Transporter Defines an Intermediate State in the Transport Cycle

(2010) Liang Feng et al.   SCIENCE

CLC Chloride Channels and Transporters: From Genes to Protein Structure, Pathology and Physiology

(2008) Thomas J. Jentsch   CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY