Search: onr:"swepub:oai:gup.ub.gu.se/298420" >
Recessive Charcot-M...
-
Sedghi, M.Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Iran
(author)
Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP
- Article/chapterEnglish2019
Publisher, publication year, extent ...
-
2019-09-03
-
Oxford University Press (OUP),2019
Numbers
-
LIBRIS-ID:oai:gup.ub.gu.se/298420
-
https://gup.ub.gu.se/publication/298420URI
-
https://doi.org/10.1093/braincomms/fcz011DOI
-
https://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17978URI
Supplementary language notes
Part of subdatabase
Classification
-
Subject category:ref swepub-contenttype
-
Subject category:art swepub-publicationtype
Notes
-
CC BY 4.0
-
Variants in MCM3AP, encoding the germinal-centre associated nuclear protein, have been associated with progressive polyneuropathy with or without intellectual disability and ptosis in some cases, and with a complex phenotype with immunodeficiency, skin changes and myelodysplasia. MCM3AP encoded protein functions as an acetyltransferase that acetylates the replication protein, MCM3, and plays a key role in the regulation of DNA replication. In this study, we report a novel variant in MCM3AP (p.Ile954Thr), in a family including three affected individuals with characteristic features of Charcot-Marie-Tooth neuropathy and multiple sclerosis, an inflammatory condition of the central nervous system without known genetic cause. The affected individuals were homozygous for a missense MCM3AP variant, located at the Sac3 domain, which was predicted to affect conserved amino acid likely important for the function of the germinal-centre associated nuclear protein. Our data support further expansion of the clinical spectrum linked to MCM3AP variant and highlight that MCM3AP should be considered in patients with accompaniment of recessive motor axonal Charcot-Marie-Tooth neuropathy and multiple sclerosis.
Subject headings and genre
Added entries (persons, corporate bodies, meetings, titles ...)
-
Moslemi, Ali-RezaGothenburg University,Göteborgs universitet,Institutionen för biomedicin,Institute of Biomedicine,Department of Pathology, Sahlgrenska University Hospital, Gothenburg University, Sweden(Swepub:gu)xmosal
(author)
-
Cabrera-Serrano, M.Department of Neurology, Hospital Universitario Virgen del Rocio, Sevilla, Spain / Instituto de Biomedicina de Sevilla, Universidad de Sevilla, Spain
(author)
-
Ansari, B.Department of neurology, Isfahan University of Medical Sciences, Iran
(author)
-
Ghasemi, M.Department of neurology, Isfahan University of Medical Sciences, Iran
(author)
-
Baktashian, M.Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Iran
(author)
-
Fattahpour, A.Radiology Resident, Department of Radiology, Mashhad University of Medical Sciences, Iran
(author)
-
Tajsharghi, HomaHögskolan i Skövde,Institutionen för hälsovetenskaper,Forskningsmiljön hälsa, hållbarhet och digitalisering,Translationell medicin TRIM, Translational Medicine(Swepub:his)tajh
(author)
-
Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, IranInstitutionen för biomedicin
(creator_code:org_t)
Related titles
-
In:Brain Communications: Oxford University Press (OUP)1:12632-1297
Internet link
Find in a library
To the university's database