A homozygous missense mutation in SCNN1A is responsible for...

AJP Endocrinology and Metabolism 2011 / 09 Vol. 301; Iss. 3

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

Dirlewanger, M., Huser, D., Zennaro, M.-C., Girardin, E., Schild, L., Schwitzgebel, V. M.
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Volume:
301
Language:
english
Journal:
AJP: Endocrinology and Metabolism
DOI:
10.1152/ajpendo.00066.2011
Date:
September, 2011
File:
PDF, 633 KB
english, 2011
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