Sturtz F

References (1)

Title : A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature - Lerat_2017_J.Peripher.Nerv.Syst_22_77
Author(s) : Lerat J , Cintas P , Beauvais-Dzugan H , Magdelaine C , Sturtz F , Lia AS
Ref : J Peripher Nerv Syst , 22 :77 , 2017
Abstract : Lerat_2017_J.Peripher.Nerv.Syst_22_77
ESTHER : Lerat_2017_J.Peripher.Nerv.Syst_22_77
PubMedSearch : Lerat_2017_J.Peripher.Nerv.Syst_22_77
PubMedID: 28448692
Gene_locus related to this paper: human-ABHD12