Associated Papers
The Genetic Perspective of Familial Glucocorticoid Deficiency: In Silico Analysis of Two Novel Variants.
Heshmatzad K et al.
International Journal of Endocrinology, 2020
Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of Literature.
Abuduxikuer K et al.
Frontiers in Endocrinology, 2019
Novel compound heterozygous mutation of the MC2R gene in a patient with familial glucocorticoid deficiency.
Matsuura H et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2006
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