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A Novel Missense PRKAR1A Variant Causes Carney Complex
Boram Kim, Han Na Jang, Kyung Shil Chae, Ho Seop Shin, Yong Hwy Kim, Su Jin Kim, Moon-Woo Seong, Jung Hee Kim
Endocrinol Metab. 2022;37(5):810-815.   Published online October 4, 2022

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A Novel Missense PRKAR1A Variant Causes Carney Complex
Endocrinology and Metabolism. 2022;37(5):810-815   Crossref logo
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Novel PRKAR1A mutation in Carney complex with cardiac myxoma
Pediatrics International. 2017;59(7):840-841   Crossref logo
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A novel PRKAR1A gene mutation in Carney complex
Clinical and Experimental Dermatology. 2021;47(2):476-479   Crossref logo
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Cushing syndrome: uncovering Carney complex due to novel PRKAR1A mutation
Endocrinology, Diabetes & Metabolism Case Reports. 2019;2019:   Crossref logo
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Association between subclinical hyperthyroidism and a PRKAR1A gene variant in Carney complex patients: A case report and systematic review
Frontiers in Endocrinology. 2022;13:   Crossref logo

A Novel PRKAR1A Mutation Associated With Primary Pigmented Nodular Adrenocortical Disease and the Carney Complex
Endocrine Practice. 2010;16(2):198-204   Crossref logo
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A novel <i>PRKAR1A</i> mutation resulting in a splicing variant in a case of Carney complex
The Korean Journal of Internal Medicine. 2015;30(5):730-734   Crossref logo
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SAT-LB48 Novel Genetic Variant of Carney Complex With Acromegaly
Journal of the Endocrine Society. 2020;4(Supplement_1):   Crossref logo
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Case report of familial Carney complex due to novel frameshift mutation c.597del C (p.Phe200LeufsX6) in PRKAR1A
Molecular Genetics and Metabolism. 2008;95(3):182-187   Crossref logo
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Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!
FEBS Letters. 2003;546(1):59-64   Crossref logo
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