Title : Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene - Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
Author(s) :
Louhichi N , Bahloul E , Marrakchi S , Othman HB , Triki C , Aloulou K , Trabelsi L , Mahfouth N , Ayadi-Mnif Z , Keskes L , Fakhfakh F , Turki H |
Ref :
Orphanet J Rare Dis , 14 :112 , 2019 |
Abstract : Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
ESTHER : Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
PubMedSearch : Louhichi_2019_Orphanet.J.Rare.Dis_14_112 |
PubMedID: 31118107 |
Gene_locus related to this paper:
human-ABHD5 |