Work

Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation – a family study

Year: 2008

Type: article

Study design: Case Report

Source: Clinical Genetics

DOI: 10.1111/j.1399-0004.2008.01022.x

Authors: F Laccone, MC Hannibal, J Neesen, W Grisold, PF Chance, H Rehder

Institutions: Medical University of Vienna, University of Washington, Kaiser-Franz-Josef-Spital

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

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke

Award: Molecular Basis of Hereditary Neuralgic Amyotrophy

OpenAlex ID: W1967729891

FWCI: 1.155

Cites: 23

Cited by: 33

Related to: 10