Codi QR

Molecular Dynamic Simulation Analysis of a Novel Missense Variant in <i>CYB5R3</i> Gene in Patients with Methemoglobinemia

<i>Background and Objective</i>: Mutations in the <i>CYB5R3</i> 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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Format: Artigo
Idioma:Inglês
Publicat: MDPI AG 2023-02-01
Col·lecció:Medicina
Matèries:
Accés en línia:https://www.mdpi.com/1648-9144/59/2/379
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!