Work

Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 gene

Year: 1997

Type: article

Study design: Case Report

Source: Muscle & Nerve

DOI: 10.1002/(sici)1097-4598(199710)20:10<1308::aid-mus14>3.0.co;2-z

Authors: Victor V. Ionasescu, Charles C. Searby, Rebecca Ionasescu, Ricardo Reisin, Victor Ruggieri, Claudia Arberas

Institutions: University of Iowa Hospitals and Clinics, Hospital General de Niños Ricardo Gutierrez

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: W2005756777

FWCI: 0.656

Cites: 20

Cited by: 20

Related to: 10