Title : Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome - Tavian_2021_Eur.J.Transl.Myol__ |
Author(s) : Tavian D , Durdu M , Angelini C , Torre E , Missaglia S |
Ref : Eur J Transl Myol , : , 2021 |
Abstract : |
PubMedSearch : Tavian_2021_Eur.J.Transl.Myol__ |
PubMedID: 33985321 |
Gene_locus related to this paper: human-ABHD5 |
Title : A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings - Eskiocak_2019_Lipids.Health.Dis_18_232 |
Author(s) : Eskiocak AH , Missaglia S , Moro L , Durdu M , Tavian D |
Ref : Lipids Health Dis , 18 :232 , 2019 |
Abstract : |
PubMedSearch : Eskiocak_2019_Lipids.Health.Dis_18_232 |
PubMedID: 31883530 |
Gene_locus related to this paper: human-ABHD5 |
Title : Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents - Durdu_2018_BMC.Med.Genet_19_88 |
Author(s) : Durdu M , Missaglia S , Moro L , Tavian D |
Ref : BMC Med Genet , 19 :88 , 2018 |
Abstract : |
PubMedSearch : Durdu_2018_BMC.Med.Genet_19_88 |
PubMedID: 29843625 |
Gene_locus related to this paper: human-ABHD5 |