A Case Report of Gordon Holmes Syndrome Due to PNPLA6 Mutation (P1-5.018)
Year: 2025
Type: article
Study design: Case Report
Source: Neurology
Authors: Eti Muharremi, Altin Kuqo, Jera Kruja
Institutions: Cooper University Hospital, Mother Teresa Hospital
Language: English
Subfield: Clinical Biochemistry
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W4409237433