Tlili A

References (1)

Title : First description of the MEGDEHL syndrome in the Tunisian population via whole-exome sequencing: Novel nonsense mutation in SERAC1 gene - Felhi_2022_Int.J.Dev.Neurosci_82_736

Author(s) : Felhi R , Monastiri K , Ben Hamida H , Ammar M , Chioukh FZ , Tabarki B , Chouchen J , Fakhfakh F , Tlili A , Mkaouar-Rebai E

Ref : Int J Developmental Neuroscience , 82 :736 , 2022

Abstract :

PubMedSearch : Felhi_2022_Int.J.Dev.Neurosci_82_736

PubMedID: 35943861

Gene_locus related to this paper: human-SERAC1

Tlili A

References (1)

1. First description of the MEGDEHL syndrome in the Tunisian population via whole-exome sequencing: Novel nonsense mutation in SERAC1 gene - Felhi_2022_Int.J.Dev.Neurosci_82_736