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Clinical and genetic characteristics of patients with monocarboxylate transporter-8 deficiency: a multicentre

Nurullah Çelik1, Korcan Demir2, Saime Ergen Dibeklioğlu3

  • 1Department of Pediatric Endocrinology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey. celiknurullah@hotmail.com.

European Journal of Pediatrics
|December 19, 2024
PubMed

Keywords:
Allan-Herndon-Dudley syndromeMCT8 deficiencyThyroid diseaseThyroid hormone transport

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