Frasquet M

References (1)

Title : Phenotypical features of two patients diagnosed with PHARC syndrome and carriers of a new homozygous mutation in the ABHD12 gene - Frasquet_2018_J.Neurol.Sci_387_134
Author(s) : Frasquet M , Lupo V , Chumillas MJ , Vazquez-Costa JF , Espinos C , Sevilla T
Ref : Journal of Neurology Sci , 387 :134 , 2018
Abstract :
PubMedSearch : Frasquet_2018_J.Neurol.Sci_387_134
PubMedID: 29571850
Gene_locus related to this paper: human-ABHD12