Work

Charcot–Marie–Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

Year: 1993

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng0993-31

Authors: Kiyoshi Hayasaka, Masato Himoro, Wataru Sato, Goro Takada, Keiichi Uyemura, Nobuyoshi Shimizu, Thomas D. Bird, P. Michael Conneally, Phillip F. Chance

Institutions: Akita University, Keio University, University of Washington, Indiana University Indianapolis, Children's Hospital of Philadelphia

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2093211495

FWCI: 8.138

Cites: 32

Cited by: 370

Related to: 10