All individuals with variants in gene EFEMP2

5 entries on 1 page. Showing entries 1 - 5.
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AscendingIndividual ID     

ID_report     

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VIP     

Data_av     

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Phenotype details     

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Owner     
00080968 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - ARCL1B Cutis laxa, autosomal recessive, type IB (OMIM:614437) 1 1 Daniel Trujillano
00103746 SUDS047 PubMed: Neubauer 2018, Journal: Neubauer 2018 - F - Switzerland Europe 33y - - - SUD SUD 1 1 Cordula Haas
00331423 17DG0797 PubMed: Maddirevula 2018 isolated case F yes - Arab - - - - skeletal dysplasia Feeding difficulties, Generalized hypotonia, Multiple joint dislocation, Delayed gross motoNo 1 1 LOVD
00442660 Pat32 PubMed: Westra 2019 - F - - - - - - - NMD - 1 1 Johan den Dunnen
00466832 Pat119 PubMed: Tuysuz 2022 - - - Turkey - - - - - OI - 1 1 Johan den Dunnen
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