Analysis of defects in GNAS and STX16 genes in a Chinese family with pseudohypoparathyroidism-Reference-Cited by-同舟云学术

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Analysis of defects in GNAS and STX16 genes in a Chinese family with pseudohypoparathyroidism

Published:2022-04 Issue:1 Volume:47 Page:
ISSN:2724-6507
Container-title:Minerva Endocrinology
language:
Short-container-title:Minerva Endocrinol

Author:

ZHAO Pingping,LIU Jingfang,CHENG Jianguo,LI Qiong,FU Songbo,WANG Yan,YANG Xiaomei,MA Xiaoni

Publisher

Edizioni Minerva Medica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://www.minervamedica.it/pdf.php?cod=R07Y2022N01A0131

Reference5 articles.

1. Pseudohypoparathyroidism and Mechanisms of Resistance toward Multiple Hormones: Molecular Evidence to Clinical Presentation

2. Hypercalcitoninaemia in pseudohypoparathyroidism type 1A and type 1B

3. Pseudohypoparathyroidism and Gsα–cAMP-linked disorders: current view and open issues

4. (Epi)genotype-Phenotype Analysis in 69 Japanese Patients With Pseudohypoparathyroidism Type I

5. Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS

Cited by 1 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. Targeted Long‐Read Sequencing Identifies a Retrotransposon Insertion as a Cause of Altered GNAS Exon A/B Methylation in a Family With Autosomal Dominant Pseudohypoparathyroidism Type 1b ( PHP1B );Journal of Bone and Mineral Research;2022-08-03

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