Diagnosis of a mild peroxisomal phenotype with next-generation sequencing

Peroxisomal biogenesis disorders (PBD) are caused by mutations in PEX genes, and are typically diagnosed with biochemical testing in plasma followed by confirmatory testing. Here we report the unusual diagnostic path of a child homozygous for PEX1 p.G843D. The patient presented with sensorineural he...

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Detalles Bibliográficos
Autores principales: Ventura, Meredith J., Wheaton, Dianna, Xu, Mingchu, Birch, David, Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Whitney, Annette E., Jones, Richard O., Moser, Ann B., Chen, Rui, Wangler, Michael F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109284/
https://www.ncbi.nlm.nih.gov/pubmed/27872819
http://dx.doi.org/10.1016/j.ymgmr.2016.10.006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109284/
https://www.ncbi.nlm.nih.gov/pubmed/27872819
http://dx.doi.org/10.1016/j.ymgmr.2016.10.006

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