Wikidata

(Q41198126)

English

Point mutations abolish 11 beta-hydroxysteroid dehydrogenase type II activity in three families with the congenital syndrome of apparent mineralocorticoid excess.

scientific article published on May 1996

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Statements

title
Point mutations abolish 11 beta-hydroxysteroid dehydrogenase type II activity in three families with the congenital syndrome of apparent mineralocorticoid excess (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8793850
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8793850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
author name string

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