All individuals with variants in gene PEX11B

4 entries on 1 page. Showing entries 1 - 4.
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00081035 - PubMed: Trujillano 2017 unaffected parents - - - - - 0 - - PBD14B;PEX14B Peroxisome biogenesis disorder 14B (OMIM:614920) 1 1 Daniel Trujillano
00387703 M027 PubMed: Hu 2019 family, 2 affected individuals, first cousin parents - yes - Kurd - 0 - - ID syndromic intellectual disability, no microcephaly 1 2 Johan den Dunnen
00396461 15011450 PubMed: Ellingford 2017 - - - United Kingdom (Great Britain) - - 0 - - CTRCT - 1 1 Johan den Dunnen
00399129 patient;Pat4 PubMed: Ebberink 2012, PubMed: Berendse 2016 - M no Netherlands white - 0 - - PBD see paper; ... 1 1 Johan den Dunnen
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