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 |