All individuals with variants in gene CREB3L1

7 entries on 1 page. Showing entries 1 - 7.
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00373326 - PubMed: Symoens 2013 The proband phenotype is described as severe and probably best corresponds to OI II/III. - - Turkey - - - - - OI - 1 1 Raymond Dalgleish
00373327 - PubMed: Guillemyn 2019 - - - Turkey - - - - - OI - 1 1 Sofie Symoens
00373328 VI-7 PubMed: Keller 2017 - - - - - - - - - OI - 1 1 Raymond Dalgleish
00373329 - PubMed: Lindahl 2018 affected individual is described as having severe OI with blue sclerae and tooth agenesis. Two unaffected siblings were carriers of the variant and two were homozygous WT. - - Somalia - - - - - OI - 1 1 Raymond Dalgleish
00373330 P1 PubMed: Cayami et al.,2019 There are three affected adult individuals in this family, each of whom is homozygous for the pathogenic variant. - - Indonesia - - - - - OI - 1 1 Raymond Dalgleish
00434982 Pat1 PubMed: Kalayci 2023 - ? ? Turkey - 00y00m - - - OI2 - 1 1 Kim Worring
00435017 Pat2 PubMed: Kalayci 2023 - ? ? Turkey - 00y00m - - - OI2 - 1 1 Kim Worring
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