A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
SourceBMC Medical Genetics, 19, (2018), pp. |, article 69
Article / Letter to editor
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BMC Medical Genetics
SubjectAll institutes and research themes of the Radboud University Medical Center; Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life Sciences
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