ArticleThe Yale journal of biology and medicine2023

Homozygous Mutations in Thyroid Peroxidase (TPO) in Hypothyroidism with Intellectual Disability, Developmental Delay, and Hearing and Ocular Anomalies in Two Families: Severe Manifestation of Untreated TPO-deficiency Poses a Diagnostic Dilemma.

Syeda Farwa Naqvi et al.PubMed ↗Full text ↗Publisher ↗

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