Newly defined peroxisomal disease with novel ACBD5 mutation
Ozlem Gorukmez1, Cengiz Havalı2, Orhan Gorukmez1
1Department of Medical Genetics, Bursa Yüksek Ihtisas Training and Research Hospital, Bursa, Turkey.
Abstract:
Peroxisomal disorders are a heterogeneous group of diseases caused by mutations in a large number of genes. One of the genetic disorders known to cause this situation is ACBD5 (Acyl-CoA binding-domain-containing-5) gene mutations that have been described in recent years. Here, we report two siblings with a novel homozygous nonsense variation (c.1297C>T, p.Arg433*) in ACBD5 (NM_145698.4) gene using Clinical Exome Sequencing (Sophia Genetics).
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