All individuals with variants in gene RNASEH1

4 entries on 1 page. Showing entries 1 - 4.
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00046789 - PubMed: Reyes 2015, Journal: Reyes 2015 2-generation family, 1 affected,unaffected heterozygous carrier parents F no - - >42y - - - PEOA see paper; ... 2 1 Johan den Dunnen
00046790 - PubMed: Reyes 2015, Journal: Reyes 2015 2-generation family, 1 affected, unaffected heterozygous carrier parents/sibs M no - - >46y - - - PEOA see paper; ... 2 1 Johan den Dunnen
00046791 - PubMed: Reyes 2015, Journal: Reyes 2015, PubMed: Legati 2016 3-generation family, 4 affecteds (3F, 1M), unaffected heterozygous carrier parents/children F yes Italy - - - - - PEOA see paper; ..., progressive external ophtalmoparesis, cerebellar signs 1 4 Johan den Dunnen
00473196 Fam107923Pat373 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, no family history F yes Iran - - - - - ? onset 48y, Facial weakness, bilateral ptosis; Hypotonia; Proximal muscle weakness & wasting; Dysarthria; Single fiber EMG: suggestive of mild neuromuscular junction disorder; Muscle biopsy: suggestive of mitochondrial myopathies; Brain MRI: suggestive of ischemia of atherosclerotic micro-vascular occlusive disease. 1 1 Johan den Dunnen
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