Work

PMP22 Thr(118)Met: recessive CMT1 mutation or polymorphism?

Year: 1997

Type: article

Source: Nature Genetics

DOI: 10.1038/ng0197-13

Authors: Eva Nelis, Bengt Holmberg, Rolf Adolfsson, Gösta Holmgren, Christine Van Broeckhoven

Institutions: University of Antwerp, Vlaams Instituut voor Biotechnologie, University Hospital of Umeå, Region Västernorrland, Umeå University

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: W2004454928

FWCI: 1.165

Cites: 13

Cited by: 42

Related to: 10