Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 gene

por Louhichi, Nacim, Bahloul, Emna, Marrakchi, Slaheddine, Othman, Houda Ben, Triki, Chahnez, Aloulou, Kawthar, Trabelsi, Lobna, Mahfouth, Nadia, Ayadi-Mnif, Zeineb, Keskes, Leila, Fakhfakh, Faiza, Turki, Hamida
Publicado 2019