A Novel Mutation in PEX11β Gene
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DOI: 10.22037/ijcn.v15i1.26129
Abstract: 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… read more here.
Keywords: pex11 gene; pex11; novel mutation; mutation pex11 ... See more keywords