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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ISSN: 15750922
Original language: English

DOI:10.1016/j.endonu.2012.07.002

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2023 October	24	15	39
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2023 August	26	28	54
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2023 April	20	3	23
2023 March	6	4	10
2023 February	23	8	31
2023 January	14	6	20
2022 December	17	18	35
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2022 September	25	9	34
2022 August	15	11	26
2022 July	11	10	21
2022 June	13	12	25
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2021 March	37	10	47
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2020 December	45	8	53
2020 November	49	7	56
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
2020 May	31	10	41
2020 April	17	14	31
2020 March	36	15	51
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2020 January	40	18	58
2019 December	48	12	60
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2019 October	40	9	49
2019 September	26	11	37
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2016 July	54	7	61
2016 June	59	8	67
2016 May	41	11	52
2016 April	33	10	43
2016 March	32	9	41
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2015 July	50	6	56
2015 June	38	5	43
2015 May	106	7	113
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2013 August	16	4	20
2013 July	24	12	36
2013 June	15	2	17
2013 May	19	9	28
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