All individuals with variants in gene GLRX5

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00307948 13DG1665 PubMed: Anazi 2017 simplex case M - - - - - - - ID see paper; ..., Profound global developmental delay, Strabismus, Blindness, Seizures, Dysphagia, Developmental regression, Recurrent respiratory infections, Microcephaly, Hypotonia, Hypsarrhythmia, Abnormal thalamic size 1 1 Johan den Dunnen
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