GNAS Epigenetic Defects and Pseudohypoparathyroidism: Time for a New Classification?
Author:
Publisher
Georg Thieme Verlag KG
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by 22 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. High-throughput Molecular Analysis of Pseudohypoparathyroidism 1b Patients Reveals Novel Genetic and Epigenetic Defects;The Journal of Clinical Endocrinology & Metabolism;2021-06-22
2. Pseudohypoparathyroidism: application of the Italian common healthcare-pathway for a homogeneous clinical approach and a shared follow up;Italian Journal of Pediatrics;2021-03-04
3. Receptor Transduction Pathways Mediating Hormone Action;Sperling Pediatric Endocrinology;2021
4. Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3;Clinical Epigenetics;2019-01-07
5. Gαs signaling controls intramembranous ossification during cranial bone development by regulating both Hedgehog and Wnt/β-catenin signaling;Bone Research;2018-11-20
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