Title | Dominant mitochondrial membrane protein-associated neurodegeneration (MPAN) variants cluster within a specific C19orf12 isoform. |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Rickman, OJ, Salter, CG, Gunning, AC, Fasham, J, Voutsina, N, Leslie, JS, McGavin, L, Cross, HE, Posey, JE, Akdemir, ZCoban, Jhangiani, SN, Lupski, JR, Baple, EL, Crosby, AH |
Journal | Parkinsonism Relat Disord |
Volume | 82 |
Pagination | 84-86 |
Date Published | 2021 01 |
ISSN | 1873-5126 |
Abstract | Mitochondria membrane protein-associated neurodegeneration (MPAN) neurodegenerative disorder is typically associated with biallelic C19orf12 variants. Here we describe a new and review candidate previous monoallelic de novo C19orf12 variants to define loss of function mutations located in the putative non-membrane spanning C19orf12 isoform as the potential basis of monoallelic MPAN. |
DOI | 10.1016/j.parkreldis.2020.10.041 |
Alternate Journal | Parkinsonism Relat Disord |
PubMed ID | 33260061 |
Grant List | G1001931 / MR / Medical Research Council / United Kingdom G1002279 / MR / Medical Research Council / United Kingdom 216279/Z/19/Z / WT / Wellcome Trust / United Kingdom UM1 HG006542 / HG / NHGRI NIH HHS / United States |