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Dataset for a case report of a homozygous PEX16 F332del mutation
This dataset provides a clinical description along with extensive biochemical and molecular characterization of a patient with a homozygous mutation in PEX16 with an atypical phenotype. This patient described in Molecular Genetics and Metabolism Reports was ultimately diagnosed with an atypical pero...
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Publicado en: | Data Brief |
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Autores principales: | , , , , , , , |
Formato: | Artigo |
Lenguaje: | Inglês |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4737951/ https://ncbi.nlm.nih.gov/pubmed/26870756 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dib.2015.12.011 |
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