Work

A previously identified missense mutation in STYXL1 is likely benign

Year: 2018

Type: article

Source: European Journal of Medical Genetics

DOI: 10.1016/j.ejmg.2018.11.016

Authors: Holger Hengel, Yvonne Schelling, Reinhard Keimer, Werner Deigendesch, Peter Bauer, Ludger Schöls

Institutions: German Center for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Deutsche Forschungsgemeinschaft

Award: G5255864586

OpenAlex ID: W2901214922

FWCI: 0.131

Cites: 3

Cited by: 2

Related to: 10