Work

MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia

Year: 2022

Type: article

Study design: Observational Study

Source: Molecular Genetics and Genomics

DOI: 10.1007/s00438-022-01910-5

Authors: Ece Selçuk, Koray Kırımtay, Benan Temizci, Şeyma Akarsu, Elif Everest, Mehmet Barış Baslo, Meltem Demirkıran, Zuhal Yapıcı, Arzu Karabay

Institutions: Istanbul Technical University, Istanbul Medeniyet University, Istanbul University, Cukurova 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

Funder: Istanbul Teknik Üniversitesi

Award: G3675022049

OpenAlex ID: W4282965257

FWCI: 0.171

Cites: 47

Cited by: 3

Related to: 10