All individuals with variants in gene PGM1

6 entries on 1 page. Showing entries 1 - 6.
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AscendingIndividual ID     

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Owner     
00225659 - - 2-generation family, 1 affected, unaffected heterozygous carrier parents M no - - - - - - CDG1T severe PGM1-CDG 1 1 Silvia Radenkovic
00225660 - - family, multiple individuals affected, unaffected heterozygous carrier parents M yes - - - - - - CDG1T severe PGM1-CDG phenotype 1 3 Silvia Radenkovic
00269338 - - - F - - - - - - - ? Muscle weakness (HP:0001324); Global developmental delay (HP:0001263); Seizures (HP:0001250); Respiratory insufficiency due to muscle weakness (HP:0002747); Optic atrophy (HP:0000648) 1 1 Andreas Laner
00289902 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 21 Mohammed Faruq
00289903 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 67 Mohammed Faruq
00304213 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
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