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Publikováno v:
Open Journal of Biological Sciences. :062-070
Dyshormonogenesis due to thyroglobulin (TG) gene mutations is a rare cause of congenital hypothyroidism with an estimated incidence of approximately 1 in 100,000 newborns.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81e8ca7d4bfe636b71a5d122a9745409
https://doi.org/10.17352/ojbs.000006
https://doi.org/10.17352/ojbs.000006
