POU1F1 mutations in combined pituitary hormone deficiency: differing spectrum of mutations in a Western-Indian cohort and systematic analysis of world literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s11102-021-01140-9.pdf
Reference43 articles.
1. Fang Q, George AS, Brinkmeier ML, Mortensen AH, Gergics P, Cheung L, Daly AZ, Ajmal A, Pérez Millán M et al (2016) Genetics of combined pituitary hormone deficiency: roadmap into the genome era. Endocr Rev. https://doi.org/10.1210/er.2016-1101
2. Gilford H (1911) Case of asexual ateleiosis. Med. Chirurg. Trans 85:305
3. Snell GD (1929) Dwarf, a new Mendelian recessive character of the house mouse. Proc Natl Acad Sci USA. https://doi.org/10.1073/pnas.15.9.733
4. Li S, Crenshaw EB 3rd, Rawson EJ, Simmons DM, Swanson LW, Rosenfeld MG (1990) Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1. Nature. https://doi.org/10.1038/347528a0
5. Tatsumi K, Miyai K, Notomi T, Kaibe K, Amino N, Mizuno Y, Kohno H (1992) Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene. Nat Genet. https://doi.org/10.1038/ng0492-56
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