HPDL Variant Type Correlates With Clinical Disease Onset and Severity

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dc.contributor.authorLee, Eun Hye
dc.contributor.authorKim\\-Mcmanus, Olivia
dc.contributor.authorYang, Jennifer H.
dc.contributor.authorHaas, Richard
dc.contributor.authorZaki, Maha S.
dc.contributor.authorAbdel\\-Salam, Ghada M. H.
dc.contributor.authorNakamura, Yuji
dc.contributor.authorAbdel\\-Hamind, Mohamed S.
dc.contributor.authorEbrahimi\\-Fakhari, Darius
dc.contributor.authorAlecu, Julian E.
dc.contributor.authorBrunetti\\-Pierri, Nicola
dc.contributor.authorSrinivasan, Varunvenkat M.
dc.contributor.authorGowda, Vykuntaraju K.
dc.contributor.authorGross, Stephanie
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorNajarzadeh Totbati, Paria
dc.contributor.authorYadavilli, Manya
dc.contributor.authorFriedman, Liana
dc.contributor.authorOjeda, Naomi Meave
dc.contributor.authorGleeson, Joseph G.
dc.date.accessioned2025-10-16T15:11:47Z
dc.date.issued2025
dc.identifier.doi10.1002/acn3.70047
dc.identifier.otherWOS:001487629300001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5016
dc.publisherWILEY
dc.sourceANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
dc.subject4\\-hydroxyphenylpyruvate dioxygenase\\-like protein
dc.subjectencephalopathy
dc.subjecthereditary spastic paraplegia
dc.subjectHPDL
dc.subjectmitochondria
dc.titleHPDL Variant Type Correlates With Clinical Disease Onset and Severity
dc.typeArticle

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