All individuals with variants in gene TRMT10A

4 entries on 1 page. Showing entries 1 - 4.
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00293496 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00361898 - - - - - - - - - - - MLD Neuroregression, hypertonia, pendular nystagmus, microcephaly 1 1 Anju Shukla
00387702 M023 PubMed: Hu 2019 family, 2 affected individuals, first cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, microcephaly 1 2 Johan den Dunnen
00433360 FamPatIV5;Pat6;Pat29 PubMed: Igoillo-Esteve 2013, PubMed: Duerinckx 2020, PubMed: Duerinckx 2021 5-generation family, 3 affected sibs, unaffected heterozygous carrier parents/relatives F yes Morocco - - - - - microcephaly primary microcephaly, young onset diabetes, short stature; OFC (SD-4), length (SD-3); 10y-generalized, absences, treatment VPA; intellectual disability; MRI normal; OFC (SD-4), length (SD-3); 10y-generalized, absences, treatment VPA; intellectual disability; MRI normal 1 3 Johan den Dunnen
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