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Neuropathy With Demyelinating Features in a Patient With Biallelic HARS1 Variants
Christina Del Greco1, Allison R Cale1, Karl Haeberlein1
1Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Journal of the Peripheral Nervous System : JPNS
|August 13, 2026
Summary
This study identifies two pathogenic variants in the HARS1 gene, leading to a complex recessive neuropathy. These findings expand the known genetic causes of HARS1-related disorders.
Area of Science:
- Genetics
- Molecular Biology
- Neurology
Background:
- The HARS1 gene encodes cytoplasmic histidyl-tRNA synthetase, crucial for protein biosynthesis.
- Pathogenic HARS1 variants are linked to Charcot-Marie-Tooth disease, ataxia, and Usher syndrome.
- HARS1 variants can cause diverse and complex neurological phenotypes.
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