A Case of Carnitine Palmitoyltransferase II Deficiency in Bahrain With a Novel Mutation

por Alsahlawi, Zahra, Fadhul, Zainab, Mahmood, Ali, Mohamed, Ali, Khalil, Mohamed, Aljishi, Emtithal
Publicado 2022

Clinical spectrum and outcome of nine patients with a novel genetic variant of galactosialidosis in the Kingdom of Bahrain

por Alsahlawi, Zahra, Aljishi, Emtithal, Kheyami, Ammar, Alekri, Ahmed, Alwedaie, Sayed Mohammed Jawad
Publicado 2022