All individuals with variants in gene NHP2

6 entries on 1 page. Showing entries 1 - 6.
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00052952 - PubMed: Vulliamy 2008, Journal: Vulliamy 2008 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Turkey - - - - - DKCB2 nail dystrophy, thrombocytopenia, testicular atrophy, opportunistic infections, growth and mental retardation, liver cirrhosis, intracranial calcification 1 1 Johan den Dunnen
00052953 - PubMed: Vulliamy 2008, Journal: Vulliamy 2008 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Turkey - >12y - - - DKCB2 12y-dyskeratosis congenita, mucocutaneous triad of nail dystrophy, leucoplakia, reticulate skin pigmentation; developed peripheral pancytopenia because of progressive bone marrow failure; no other somatic abnormalities reported 2 1 Johan den Dunnen
00334320 - PubMed: Luo 2021, Journal: Luo 2021 analysis 233 patients - - China - - - - - IMD74 hospitalized after COVID-19 infection, 1 1 Liu Wenbing
00334368 - PubMed: Luo 2021, Journal: Luo 2021 analysis 233 patients - - China - - - - - IMD74 hospitalized after COVID-19 infection, 1 1 Liu Wenbing
00334543 - PubMed: Luo 2021, Journal: Luo 2021 analysis 233 patients - - China - - - - - IMD74 hospitalized after COVID-19 infection, 1 1 Liu Wenbing
00335014 - PubMed: Luo 2021, Journal: Luo 2021 analysis 233 patients - - China - - - - - IMD74 hospitalized after COVID-19 infection, 1 1 Liu Wenbing
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