Mice lacking renal chloride channel, CLC-5, are a model for Dent’s disease, a nephrolithiasis disorder associated with defective receptor-mediated endocytosis

By Wang Sha Sha   Devuyst Olivier  

Human Molecular Genetics, Vol. 9, Iss. 20, 2000-12 ,pp. : 2937-2945

Oxford University Press

Access to resources Recommend Favorite

Characterisation of Renal Chloride Channel, CLCN5 , Mutations in Hypercalciuric Nephrolithiasis (Kidney Stones) Disorders

By Lloyd Sarah E.  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1233-1239

Oxford University Press

Access to resources Recommend Favorite

Identification of Functionally Important Regions of the Muscular Chloride Channel ClC-1 by Analysis of Recessive and Dominant Myotonic Mutations

By Wollnik Bernd   Kubisch Christian   Steinmeyer Klaus   Pusch Michael  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-01 ,pp. : 805-811

Oxford University Press

Access to resources Recommend Favorite

ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence

By Kubisch C.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1753-1760

Oxford University Press

Access to resources Recommend Favorite

Age distribution patterns of human gene families: divergent for Gene Ontology categories and concordant between different subcellular localizations

By Liu Gangbiao   Zou Yangyun   Cheng Qiqun   Zeng Yanwu   Gu Xun   Su Zhixi  

Molecular Genetics and Genomics, Vol. 289, Iss. 2, 2014-04 ,pp. : 137-147

Springer Publishing Company

Access to resources Recommend Favorite