Orphanet: Diagnóstico del hiperaldosteronismo familiar tipo III gen KCNJ5

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Diagnosis of familial hyperaldosteronism type III (KCNJ5 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 09/12/2016
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Last update: December 2016

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (1)
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