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Article

A novel PRKAR1A gene mutation associated with primary pigmented nodular adrenocortical disease.

The American journal of the medical sciences - 1 Aug 2014

Ran Hui, Ma Xiaokun, Wang Qingzhu, Xie Ziyi, Qin Guijun

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PMID: 24978147
DOI: 10.1097/MAJ.0000000000000296

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A novel PRKAR1A gene mutation associated with primary pigmented nodular adrenocortical disease.PMID 24978147Read ↗

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A novel PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease and the Carney complex.Semantic proximity Read ↗

The clinical characteristics and pathogenic variants of primary pigmented nodular adrenocortical disease in 210 patients: a systematic review.Semantic proximity Read ↗

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[A pedigree study of a patient with primary pigmented nodular adrenocortical disease and familial gene mutation].Semantic proximity Read ↗

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.Semantic proximity Read ↗

A novel splice site mutation of the PRKAR1A gene, C.440+5 G>C, in a Chinese family with Carney complex.Semantic proximity Read ↗

Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysiology: augmented PKA signaling is associated with adrenal tumorigenesis in PPNAD.Semantic proximity Read ↗

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