Literature DB >> 31420593

A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.

Fulya Akçimen1, Atay Vural2, Hacer Durmuş3, Arman Çakar3, Henry Houlden4, Yeşim G Parman3, A Nazlı Başak5.   

Abstract

Distal hereditary motor neuronopathies (dHMN) are a genetically heterogeneous group of neuromuscular disorders caused by anterior horn cell degeneration and progressive distal muscle weakness. A heterozygous missense variant in FBXO38 has been previously described in two families affected by autosomal-dominant dHMN. In this paper, we describe a homozygous missense variant in FBXO38 (c.1577G>A; p.(Arg526Gln)) in a young Turkish female, offspring of consanguineous parents, with a congenital mild neuronopathy with idiopathic toe walking, normal sensory examination, and hearing loss. This work is the first to describe a novel homozygous variant and a suggested loss of function mechanism in FBXO38, expanding the dHMN type IID phenotype.

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Year:  2019        PMID: 31420593     DOI: 10.1038/s10038-019-0652-y

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  3 in total

1.  FBXO38 Ubiquitin Ligase Controls Centromere Integrity via ZXDA/B Stability.

Authors:  Nikol Dibus; Vladimir Korinek; Lukas Cermak
Journal:  Front Cell Dev Biol       Date:  2022-06-23

2.  FBXO38 Ubiquitin Ligase Controls Sertoli Cell Maturation.

Authors:  Nikol Dibus; Eliska Zobalova; Mario A M Monleon; Vladimir Korinek; Dominik Filipp; Jana Petrusova; Radislav Sedlacek; Petr Kasparek; Lukas Cermak
Journal:  Front Cell Dev Biol       Date:  2022-06-13

3.  A Missense Mutation in the KLF7 Gene Is a Potential Candidate Variant for Congenital Deafness in Australian Stumpy Tail Cattle Dogs.

Authors:  Fangzheng Xu; Shuwen Shan; Susan Sommerlad; Jennifer M Seddon; Bertram Brenig
Journal:  Genes (Basel)       Date:  2021-03-24       Impact factor: 4.096

  3 in total

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