All individuals with variants in gene LRRC32

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AscendingIndividual ID     

ID_report     

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Owner     
00395594 RP-2005 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease congenital blindness, exudative vitreoretinopathy, nystagmus, retinal detachment, strabismus, absent septum pellucidum, heterotopia, hypoplasia of the corpus callosum, inferior vermis hypoplasia, ventriculomegaly, global developmental delay, intellectual disability, joint hypermobility, agenesis of the palate 1 1 LOVD
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