Last Updated: 09/26/2026
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Found 3 publications
Epidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America.
Journal: BMJ open
Published: September 19, 2020
Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly.
Journal: Journal of medical genetics
Published: June 28, 2019
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Last Updated: 09/26/2026