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Baumann, M.* ; Schreiber, H.* ; Schlotter-Weigel, B.* ; Löscher, W.N.* ; Stucka, R.* ; Karall, D.* ; Strom, T.M. ; Bauer, P.* ; Krabichler, B.* ; Fauth, C.* ; Glaeser, D.* ; Senderek, J.*

MPV17 mutations in juvenile- and adult-onset axonal sensorimotor polyneuropathy.

Clin. Genet. 95, 182-186 (2018)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
MPV17 encodes a putative channel-forming protein of the inner mitochondrial membrane and is involved in mitochondrial deoxynucleotide homeostasis. MPV17 mutations were first reported in patients with Navajo neurohepatopathy, an autosomal recessive mitochondrial DNA depletion syndrome, characterized by early-onset liver failure, failure to thrive as well as central and peripheral neurological involvement. Recently, two patients with juvenile-onset peripheral sensorimotor neuropathy associated with an MVP17 c.122G>A (p.Arg41Gln) variant have been reported. Here, we describe five additional patients from two unrelated families with sensorimotor axonal neuropathy without hepatocerebral affection caused by homozygous MPV17 variants. Patients of the first family carried the known c.122G>A variant and affected individuals of the second family had a novel c.376-9T>G near-splice variant, which was shown to result in an in-frame deletion of 11 amino acids. This report provides further evidence that MPV17 mutations should be considered in patients with pure, non-syndromic axonal neuropathy.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Axonal Sensorimotor Polyneuropathy ; Mitochondrial Dna Depletion Syndrome 6 ; Mpv17 ; Mtdps6 ; Navajo Neurohepatopathy ; Nnh; Neurohepatopathy; Neuropathy; Protein
Sprache englisch
Veröffentlichungsjahr 2018
HGF-Berichtsjahr 2018
ISSN (print) / ISBN 0009-9163
e-ISSN 1399-0004
Zeitschrift Clinical Genetics
Quellenangaben Band: 95, Heft: 1, Seiten: 182-186 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort 111 River St, Hoboken 07030-5774, Nj Usa
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Human Genetics (IHG)
POF Topic(s) 30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-500700-001
DOI 10.1111/cge.13462
WOS ID WOS:000453219300018
PubMed ID 30298599
Erfassungsdatum 2018-10-23
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