A case of systemic pseudohypoaldosteronism with a novel mutation in the SCNN1A gene

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Un caso de pseudohipoaldosteronismo sistémico con una mutación nueva en el gen SCNN1A

Nicole Silvaa,

Corresponding author

nicolemad@gmail.com

Corresponding author.

, Miguel Costaa, Albina Silvaa, Carla Sáa, Sofia Martinsb, Ana Antunesb, Olinda Marquesb, Sérgio Castedoc, Almerinda Pereiraa

a Neonatal Intensive Care Department, Hospital Braga, Braga, Portugal

b Pediatric Department, Division of Pediatric Endocrinology, Hospital Braga, Braga, Portugal

c GDPN, Genética Médica e Diagnóstico Pré – Natal, Prof. Doutor Sérgio Castedo, Porto, Portugal

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Article information

ISSN: 15750922
Original language: English

DOI:10.1016/j.endonu.2012.07.002

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2023 April	20	3	23
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2021 March	37	10	47
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2020 December	45	8	53
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2020 October	28	7	35
2020 September	28	10	38
2020 August	35	9	44
2020 July	30	13	43
2020 June	33	7	40
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2013 November	15	7	22
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2013 July	24	12	36
2013 June	15	2	17
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