(Q60624098)

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A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1

article published in 2011

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A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 (English)

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Maria-Christina Zennaro

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3

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Europe PubMed Central

PubMed ID

21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

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26 May 2020

Valerie M Schwitzgebel

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6

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Europe PubMed Central

PubMed ID

21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

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26 May 2020

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Mirjam Dirlewanger

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1

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Europe PubMed Central

PubMed ID

21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 May 2020

Delphine Huser

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2

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Europe PubMed Central

PubMed ID

21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

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26 May 2020

Eric Girardin

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4

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21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

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26 May 2020

Laurent Schild

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5

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21653223

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26 May 2020

publication date

September 2011

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American Journal of Physiology - Endocrinology and Metabolism

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Europe PubMed Central

PubMed ID

21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 May 2020

volume

301

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21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

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26 May 2020

page(s)

E467-73

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Europe PubMed Central

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21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

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26 May 2020

issue

3

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Europe PubMed Central

PubMed ID

21653223

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 May 2020

Identifiers

DOI

10.1152/AJPENDO.00066.2011

1 reference

stated in

Europe PubMed Central

PubMed ID

21653223

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

26 May 2020

1 reference

Europe PubMed Central

PubMed ID

21653223

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21653223%20AND%20SRC:MED&resulttype=core&format=json

(Q60624098)

A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1

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