Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot–Marie–Tooth disease

Author:

Brennan Kathryn M.,Bai Yunhong,Pisciotta Chiara,Wang Suola,Feely Shawna M.E.,Hoegger Mark,Gutmann Laurie,Moore Steven A.,Gonzalez Michael,Sherman Diane L.,Brophy Peter J.,Züchner Stephan,Shy Michael E.

Funder

Inherited Neuropathy Consortium-Rare Disease Clinical Research Consortium

National Institute of Neurological Disorders and Stroke

National Center for Advancing Translational Sciences

Muscular Dystrophy Association

Charcot-Marie-Tooth Association

National Institutes of Health

Wellcome Trust

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference27 articles.

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2. Les étranglements de Ranvier et les espaces interannulaires des fibres nerveuses a myéline;Nageotte;Comp Rend l Assoc Anat,1910

3. Über die beziehung der sog. “zellen der schwannschen scheide” zum myelin in den nervenfasen von säugetieren;Nemiloff;Arch Mikrosk Anat Entwicklungsgesch,1910

4. El aparato endocelular de Golgi de la célula de Schwann y algunas observaciones sobre la estructura de los tubos nerviosos;Ramόn y Cajal;Trab Lab Invest Biol Univ Madrid,1912

5. A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease;Guilbot;Hum Mol Genet,2001

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