Work

Clinical Report Homozygous SMN1 Deletions in Unaffected Family Members and Modification of the Phenotype by SMN2

Year: 2004

Type: article

Study design: Case Report

Authors: Thomas W. Prior, Kathryn J. Swoboda, H. Denman Scott, Ashley Q. Hejmanowski

Language: English

Topic: Neurogenetic and Muscular Disorders Research

Subfield: Genetics

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W301264335

FWCI:

Cites: 16

Cited by:

Related to: 10