Cargando…
MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing
BACKGROUND: Correct diagnosis is pivotal to understand and treat neurological disease. Herein, we report the diagnostic work-up utilizing exome sequencing and the characterization of clinical features and brain MRI in two siblings with a complex, adult-onset phenotype; including peripheral neuropath...
Autores principales: | Haugarvoll, Kristoffer, Johansson, Stefan, Tzoulis, Charalampos, Haukanes, Bjørn Ivar, Bredrup, Cecilie, Neckelmann, Gesche, Boman, Helge, Knappskog, Per Morten, Bindoff, Laurence A |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567975/ https://www.ncbi.nlm.nih.gov/pubmed/23286897 http://dx.doi.org/10.1186/1750-1172-8-1 |
Ejemplares similares
-
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
por: Tzoulis, Charalampos, et al.
Publicado: (2013) -
Asymptomatic retinal dysfunction in alpha-methylacyl-CoA racemase deficiency
por: Alsalamah, Abrar K., et al.
Publicado: (2021) -
Diagnostic utility of a-methylacyl COA racemase in prostate cancer of the Iranian population
por: Taheri, Diana, et al.
Publicado: (2021) -
Expression and Characterization of α-Methylacyl CoA Racemase from Anisakis simplex Larvae
por: Kim, Bong Jin, et al.
Publicado: (2012) -
Alpha-Methylacyl-CoA Racemase (AMACR), a Potential New Biomarker for Glioblastoma
por: Lee, Hyunji, et al.
Publicado: (2020)