Joubert syndrome caused by a TMEM67 mutation: Genotype-phenotype analysis.

Autor: Neissi, Mostafa1,2,3 iammostafaneissi@gmail.com, Mohammadi-Asl, Misagh3, Roghani, Mojdeh3, Al-Badran, Adnan Issa4, Sheikh-Hosseini, Motahareh3,5, Mohammadi-Asl, Javad3,6
Zdroj: Neurology Asia. 2024, Vol. 29 Issue 2, p501-506. 6p.
Databáze: Academic Search Ultimate