All individuals with variants in gene MTFMT

13 entries on 1 page. Showing entries 1 - 13.
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VIP     

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Owner     
00003019 - PubMed: Neveling 2013 - - - - - - - - - ? PMR, epilepsy, myopathy, dystonia Leigh syndrome 2 1 Marcel Nelen
00036271 - - - - - Germany - - - - - ? suspected Morbus Leigh 1 1 Andreas Laner
00036272 - - - - - Germany - - - - - ? suspected Morbus Leigh 1 1 Andreas Laner
00036273 - - - - - Germany - - - - - ? suspected Morbus Leigh 1 1 Andreas Laner
00274200 Pat91 PubMed: Pronicka 2016 - M - Poland - - - - - ? deceased; mitochondrial disease criteria score 6; muscle biopsy 2 1 Johan den Dunnen
00291275 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00291276 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00291277 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 177 Mohammed Faruq
00296585 Pat18 PubMed: Kemp 2011, PubMed: Taylor 2014 2 affected F - Germany - - - - - ? muscle not affected; central nervous system not affected; heart not affected; liver not affected; lactic acidosis 2 2 Johan den Dunnen
00296586 Pat19 PubMed: Taylor 2014 - F - United Kingdom (Great Britain) British - - - - ? muscle affected; central nervous system affected; heart affected; liver not affected; mild sensory neuropathy 2 1 Johan den Dunnen
00303626 Family_36 PubMed: Makrythanasis 2014 family, 2 affected - yes Egypt - - - - - ? see paper; ..., syndromic intellectual disability/developmental delay 1 2 Johan den Dunnen
00304475 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 12 Mohammed Faruq
00454707 NGSP18 PubMed: Legati 2016 - F - - - - - - - mitochondrial pshycomotor delay, dystonia, Leigh syndrome 2 1 Daniele Ghezzi
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