MKRN3 circulating levels in Prader–Willi syndrome: a pilot study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s40618-022-01860-0.pdf
Reference30 articles.
1. Cassidy SB, Schwartz S, Miller JL, Driscoll DJ (2012) Prader–Willi syndrome. Genet Med 14:10–26
2. Butler MG (2011) Prader–Willi syndrome: obesity due to genomic imprinting. Curr Genomics 12:204–215
3. Angulo MA, Butler MG, Cataletto ME (2015) Prader–Willi syndrome: a review of clinical, genetic, and endocrine findings. J Endocrinol Invest 38:1249–1263
4. Heksch R, Kamboj M, Anglin K, Obrynba K (2017) Review of Prader–Willi syndrome: the endocrine approach. Transl Pediatr 6(4):274–285
5. Costa RA, Ferreira IR, Cintra HA et al (2019) Genotype-phenotype relationships and endocrine findings in Prader–Willi syndrome. Front Endocrinol (Lausanne) 13(10):864
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1. Genotype–phenotype characteristics of 57 patients with Prader–Willi syndrome: a single-center experience from Turkey;Clinical Dysmorphology;2024-06-18
2. Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation;Frontiers in Endocrinology;2024-04-26
3. MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutations;Journal of Endocrinological Investigation;2023-12-19
4. MKRN3 role in regulating pubertal onset: the state of art of functional studies;Frontiers in Endocrinology;2022-09-16
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