Mutations in KCNJ5 determines presentation and likelihood of cure in primary hyperaldosteronism

Publisher： John Wiley & Sons Inc

E-ISSN： 1445-2197|85|4|279-283

ISSN： 1445-1433

Source： ANZ JOURNAL OF SURGERY, Vol.85, Iss.4, 2015-04, pp. : 279-283

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype

By  

CLINICAL ENDOCRINOLOGY, Vol. 83, Iss. 6, 2015-12 ,pp. : 779-789

John Wiley & Sons Inc

Access to resources Recommend Favorite

Hyperkeratosis lenticularis perstans in a patient with primary hyperaldosteronism

By  

JOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, Vol. 16, Iss. 1, 2018-01 ,pp. : 72-73

John Wiley & Sons Inc

Access to resources Recommend Favorite

Is Primary Hyperaldosteronism a Risk Factor for Aortic Dissection?

By  

Cardiology, Vol. 108, Iss. 1, 2006-09 ,pp. : 48-50

Karger

Access to resources Recommend Favorite

Primary Aldosteronism: the spectre of cure

By  

CLINICAL ENDOCRINOLOGY, Vol. 82, Iss. 6, 2015-06 ,pp. : 785-788

John Wiley & Sons Inc

Access to resources Recommend Favorite

CDKN2A mutations could influence the dermoscopic pattern of presentation of multiple primary melanoma: a clinical dermoscopic genetic study

By  

JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY & VENEREOLOGY, Vol. 29, Iss. 3, 2015-03 ,pp. : 574-580

John Wiley & Sons Inc

Access to resources Recommend Favorite