Work

Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1

Year: 1999

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/302609

Authors: Carol Hardy, Farhat Khanim, Rosarelis Torres, Martin Scott-Brown, Anneke Seller, Joanna Poulton, David Collier, Jeremy Kirk, Mihael Polymeropoulos, Farida Latif, Timothy Barrett

Institutions: Birmingham Women's Hospital, University of Birmingham, George Washington University, Novartis (United States), Churchill Hospital, John Radcliffe Hospital, Birmingham Children's Hospital

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: bronze

OpenAlex ID: W1975301556

FWCI: 3.783

Cites: 22

Cited by: 212

Related to: 10