Cargando…
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia
Background and Objective: Mutations in the CYB5R3 gene cause reduced NADH-dependent cytochrome b5 reductase enzyme function and consequently lead to recessive congenital methemoglobinemia (RCM). RCM exists as RCM type I (RCM1) and RCM type II (RCM2). RCM1 leads to higher methemoglobin levels causing...
Autores principales: | Ullah, Asmat, Shah, Abid Ali, Syed, Fibhaa, Mahmood, Arif, Ur Rehman, Hassan, Khurshid, Beenish, Samad, Abdus, Ahmad, Wasim, Basit, Sulman |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9967277/ https://www.ncbi.nlm.nih.gov/pubmed/36837579 http://dx.doi.org/10.3390/medicina59020379 |
Ejemplares similares
-
Neurological and Neuroimaging Features of CYB5R3-Related Recessive Hereditary Methemoglobinemia Type II
por: Nicita, Francesco, et al.
Publicado: (2022) -
Identification of novel inhibitors for SARS-CoV-2 as therapeutic options using machine learning-based virtual screening, molecular docking and MD simulation
por: Samad, Abdus, et al.
Publicado: (2023) -
c.151dup variant in LAMA3 in Pakistani patients affected with Shabbir Syndrome but showing mild symptoms
por: Ullah, Asmat, et al.
Publicado: (2023) -
Dilated Cardiomyopathy due to the Novel MT-CYB Missense Mutation m.14757T>C
por: Zarrouk, Sinda, et al.
Publicado: (2021) -
A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1()
por: Hajra, Bibi, et al.
Publicado: (2023)