All individuals with variants in gene MGME1

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

ID_report     

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VIP     

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Owner     
00081068 - PubMed: Trujillano 2017 no information from parents - - - - - - - - MTDPS11 m DNA depletion syndrome 11 (OMIM:615084) 1 1 Daniel Trujillano
00292873 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 14 Mohammed Faruq
00292874 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 6 Mohammed Faruq
00292875 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00296587 Pat20 PubMed: Taylor 2014 - M - United Kingdom (Great Britain) British 2y6m - - - ? deceased; muscle not affected; central nervous system not affected; heart affected; liver not affected; mtDNA depletion 2 1 Johan den Dunnen
00314364 - PubMed: Topf 2020 analysis 1001 patients with unexplained limb-girdle weakness - - - - - - - - LGMD - 1 2 Johan den Dunnen
00431386 - - - F likely Brazil - - - - - MTDPS11 - 1 350 Eduardo Estephan
00473155 Fam103277Pat301 PubMed: Molaei 2025 analysis 2009 neuromuscular disorder individuals; patient, family history M yes Iran - - - - - MYOP onset 18y with bilateral ptosis; External ophtalmoplegia; Poor vision; Facial muscle weakness; Mild lower & upper limbs muscle weakness; Exercise intolerance; Generalized neuropathy; Pes cavus; Hair loss & Alopecia; itchy-Rash; Elevated level of CPK; EMG: Non-irritable myopathy; Muscle biopsy compatible with mitochondrial myopathy; Positive Hx. of Lichen Planus. 1 1 Johan den Dunnen
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