Cargando…
Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approach
BACKGROUND: Methylmalonic acidemia (MMA) is a rare metabolic disorder resulting from functional defects in methylmalonyl-CoA mutase. Mutations in the MMAB gene are responsible for the cblB type of vitamin B12-responsive MMA. RESULTS: This study used Whole-exome sequencing (WES), Sanger sequencing, l...
Autores principales: | Maryami, Fereshteh, Rismani, Elham, Davoudi-Dehaghani, Elham, Khalesi, Nasrin, Motlagh, Fatemeh Zafarghandi, Kordafshari, Alireza, Talebi, Saeed, Rahimi, Hamzeh, Zeinali, Sirous |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10226198/ https://www.ncbi.nlm.nih.gov/pubmed/37248539 http://dx.doi.org/10.1186/s41065-023-00281-0 |
Ejemplares similares
-
Characterization of Niemann-Pick diseases genes mutation spectrum in Iran and identification of a novel mutation in SMPD1 gene
por: Zahedi Abghari, Fateme, et al.
Publicado: (2019) -
A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population
por: Maryami, Fereshteh, et al.
Publicado: (2015) -
Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient
por: Alaei, Mohammad Reza, et al.
Publicado: (2020) -
Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect
por: Mojbafan, Marzieh, et al.
Publicado: (2019) -
Molecular Basis of α-Thalassemia in Iran
por: Valaei, Atefeh, et al.
Publicado: (2018)