All individuals with variants in gene ACAT1

5 entries on 1 page. Showing entries 1 - 5.
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00290209 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 23 Mohammed Faruq
00438640 HSJ0048 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) M - Canada French-Canadian - - - pharmaco-resistant seizures DEE see paper; ..., severe global developmental delay, severe intellectual disability; 11m-seizures; EEG modified hypsarrhythmia; MRI brain increased sub-arachnoid spaces; axial and limb hypotonia, hyporeflexia, scoliosis, hypersalivation 1 1 Johan den Dunnen
00450485 3bINP-017 PubMed: Vela-Amieva 2024 Brother affected (died at 20y11m) F no Mexico Mexican - - - - aciduria, alpha-methylacetoacetic Cubitus valgus 2 1 Miriam Erandi Reyna-Fabián
00451615 3bINP-047 PubMed: Vela-Amieva 2024 Likely consanguinity. Co-occurrence of two different monogenic diseases (a pathogenic variant in the TTN gene was identified as a secondary finding). F no Mexico Mexican - - - - aciduria, alpha-methylacetoacetic - 1 1 Miriam Erandi Reyna-Fabián
00453608 Pat24 PubMed: Navarrete 2019 newborn screening - - Spain - - - - - metabolic syndrome see paper; ..., newborn screening tandem mass spectrometry dried blood spots 1 1 Johan den Dunnen
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