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Clinical and Genetic Characteristics of Patients with Monocarboxylate Transporter-8 Deficiency: a Multicentre Retrospective Study.

Nurullah Çelik,Korcan Demir, Saime Ergen Dibeklioğlu, Bumin Nuri Dündar,Nihal Hatipoğlu,Gül Yeşiltepe Mutlu,Emrullah Arslan, Didem Yıldırımçakar,Atilla Çayır, Bülent Hacıhamdioğlu,Zümrüt Kocabey Sütçü, Yağmur Ünsal,Gülay Karagüzel

European Journal of Pediatrics(2024)

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关键词
MCT8 deficiency,Allan-Herndon-Dudley syndrome,Thyroid disease,Thyroid hormone transport
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