Associated Papers
Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia.
Chen L et al.
Translational Psychiatry, 2024
38951484 (PubMed )
Supplement: 41398_2024_2984_MOESM1_ESM.pdf
The Prevalence, Clinical, and Molecular Characteristics of Congenital Hypothyroidism Caused by DUOX2 Mutations: A Population-Based Cohort Study in Guangzhou.
Tan M et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme, 2016
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