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A Novel Mutation in PEX11β Gene
PEX11β ([OMIM] 614920) mutation causes an extremely rare subgroup of peroxisomal biogenesis disorders, with only six cases reported to date. In this article, we reported a patient with episodic migraine-like attacks, delirium, mood and behavior change, polyneuropathy, and history of congenital catar...
Autores principales: | MALEKZADEH, Hamid, SHAKIBA, Marjan, YASAEI, Mehrdad |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shahid Beheshti University of Medical Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856433/ https://www.ncbi.nlm.nih.gov/pubmed/33558817 http://dx.doi.org/10.22037/ijcn.v15i1.26129 |
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