Cargando…
Genetic testing of leukodystrophies unraveling extensive heterogeneity in a large cohort and report of five common diseases and 38 novel variants
This study evaluates the genetic spectrum of leukodystrophies and leukoencephalopathies in Iran. 152 children, aged from 1 day to 15 years, were genetically tested for leukodystrophies and leukoencephalopathies based on clinical and neuroradiological findings from 2016 to 2019. Patients with a sugge...
Autores principales: | Mahdieh, Nejat, Soveizi, Mahdieh, Tavasoli, Ali Reza, Rabbani, Ali, Ashrafi, Mahmoud Reza, Kohlschütter, Alfried, Rabbani, Bahareh |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864965/ https://www.ncbi.nlm.nih.gov/pubmed/33547378 http://dx.doi.org/10.1038/s41598-021-82778-0 |
Ejemplares similares
-
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche
por: Soveizi, Mahdieh, et al.
Publicado: (2020) -
A novel PKP2 mutation and intrafamilial phenotypic variability in ARVC/D
por: Mahdieh, Nejat, et al.
Publicado: (2018) -
21-Hydroxylase Deficiency: Newborn Screening in Iran?
por: Mahdieh, Nejat, et al.
Publicado: (2012) -
An Overview of Mutation Detection Methods in Genetic Disorders
por: Mahdieh, Nejat, et al.
Publicado: (2013) -
The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants
por: Heshmatzad, Katayoun, et al.
Publicado: (2020)