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 |
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Zdroj: | Neurology Asia. 2024, Vol. 29 Issue 2, p501-506. 6p. |
Databáze: | Academic Search Ultimate |
Externí odkaz: |