- Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran
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Komachali SR, Siahpoosh Z, Salehi M
- KMID: 2535365
- Genomics Inform.
- 2022 Sep;20(3):e30.
- doi: 10.5808/gi.22030
Hereditary spastic paraplegia is a not common inherited neurological disorder with heterogeneous clinical expressions. ALDH18A1 (located on 10q24.1) gene-related spastic paraplegias (SPG9A and SPG9B) are rare metabolic disorders caused by... -
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