학술논문
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
Document Type
Article
Source
In: Yale Journal of Biology and Medicine . (Yale Journal of Biology and Medicine, 2023, 96(3):347-365)
Subject
Language
English
ISSN
15514056
00440086
00440086