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Novel SLC16A2 Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism, Allan–Herndon–Dudley Syndrome

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Bibliographic Details
Published in:	Neurology India 2023-11, Vol.71 (6), p.1282-1283
Main Authors:	Mahesan, Aakash, Kamila, Gautam, Choudhary, Puneet, Jauhari, Prashant, Chakrabarty, Biswaroop, Kumar, Atin, Gulati, Sheffali
Format:	Article
Language:	English
Citations:	Items that this one cites
Online Access:	Get full text
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