Case Report
Published on 28 Feb 2022
Case Report: A Novel Point Mutation of SOX3 in a Subject With Growth Hormone Deficiency, Hypogonadotrophic Hypogonadism, and Borderline Intellectual Disability
in Pediatric Endocrinology
Frontiers in Endocrinology
doi 10.3389/fendo.2022.810375
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- 6 citations