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pro vyhledávání: '"Hannes Köpke"'
Autor:
Sivaraj M Sundaram, Adriana Arrulo Pereira, Helge Müller-Fielitz, Hannes Köpke, Meri De Angelis, Timo D Müller, Heike Heuer, Jakob Körbelin, Markus Krohn, Jens Mittag, Ruben Nogueiras, Vincent Prevot, Markus Schwaninger
Publikováno v:
Brain 145, 4264-4274 (2022)
A genetic deficiency of the solute carrier monocarboxylate transporter 8 (MCT8), termed Allan-Herndon-Dudley syndrome, is an important cause of X-linked intellectual and motor disability. MCT8 transports thyroid hormones across cell membranes. While
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b625c625d11d5d30c7fad13c5f1e896
https://www.ncbi.nlm.nih.gov/pubmed/35929549
https://www.ncbi.nlm.nih.gov/pubmed/35929549
