All individuals with variants in gene SCO2

8 entries on 1 page. Showing entries 1 - 8.
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00036997 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00050428 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? generalized hypotonia, global developmental delay 1 1 Johan den Dunnen
00274182 Pat54 PubMed: Pronicka 2016 - M - Poland - - - - - ? deceased; mitochondrial disease criteria score 6; muscle biopsy 1 1 Johan den Dunnen
00293157 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00296593 Pat26 PubMed: Taylor 2014 - F - Poland - 18m - - - ? deceased; muscle affected; central nervous system affected; heart not affected; liver not affected; failure to thrive, elevated cerebrospinal fluid lactate 1 1 Johan den Dunnen
00377599 161234 - - M likely - Persian - - - - CEMCOX1 Neuromuscular disease or hereditary sensory-motor neuropathy (axonal) with paraparesis of the legs, contractures of the ankle and metacarpophalangeal joints of the thumb, atrophy of the calf and foot muscles as well as the hand muscles, tongue fasciculations, tremor of the hands, Pes cavus on both sides, loss of the ability to walk at the age of 11. Younger brother with possible onset of similar symptoms 1 1 Andreas Laner
00446782 Pat58 PubMed: Miszalski-Jamka 2017 case not solved - - - - - - - - LVNC - 1 1 Johan den Dunnen
00446810 Pat96 PubMed: Miszalski-Jamka 2017 case not solved - - - - - - - - LVNC - 1 1 Johan den Dunnen
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