Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.
| Autor: | Ghanei, Mahmoud1,2, Sadat Fatemi, Seyedeh Helia1,2, Soudyab, Mohammad1, Esfehani, Reza Jafarzadeh2 drrezajafarzadeh@yahoo.com |
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| Zdroj: | Neurology Asia. 2022, Vol. 27 Issue 4, p955-962. 8p. |
| Databáze: | Academic Search Ultimate |
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