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Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran
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Genomics Inform. 2022;20(3):e30 Published online 2022 Sep 30 DOI: https://doi.org/10.5808/gi.22030
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Citations to this article as recorded by
 Review of the Genetic Spectrum of Hereditary Spastic Paraplegias in the Middle East and North Africa Regions
Mehri Salari, Fatemeh Hojjatipour, Masoud Etemadifar, Sevim Soleimani
Neurology Genetics.2025;[Epub] CrossRef Editorial for the special collection: frontiers in rare disease genetics
Murim Choi
Genomics & Informatics.2025;[Epub] CrossRef
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