Rare variants in the YKT6 gene cause new neurological disorder, study finds
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A recent collaborative study has discovered rare variants in the YKT6 gene as the cause of a new neurological disorder…
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma
Overview of attention for article published in Genetics in Medicine, March 2024
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