All individuals with variants in gene VRK1

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

ID_report     

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00081058 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - PCH1A Pontocerebellar hypoplasia type 1A (OMIM:607596) 1 1 Daniel Trujillano
00291152 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304454 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00361548 11DG0443 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID not syndromic; global developmental delay, microlissencephaly 1 1 Johan den Dunnen
00374534 S-569 PubMed: Ganapathy 2019 - - - India - - - - - ? Bilateral foot drop and high stepping gait, difficulty in getting up from squatting position and weak bilateral interosseous nerve, suggesting axonal neuropathy 1 1 Johan den Dunnen
00375664 Pat74 PubMed: Srivastava 2014 - - - United States - - - - - ? progressive; intellectual disability/developmental delay; microcephaly; hypophonia, dysarthria; decreased muscle bulk, hypotonia, weakness, tremor, dysmetria, broad-based gait; hyper-reflexia; MRI brain normal 1 1 Johan den Dunnen
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