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.

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.

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