A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 (Q60624098)
Jump to navigation
Jump to search
article published in 2011
Language | Label | Description | Also known as |
---|---|---|---|
English | A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 |
article published in 2011 |
Statements
A homozygous missense mutation in SCNN1A is responsible for a transient neonatal form of pseudohypoaldosteronism type 1 (English)
0 references
Mirjam Dirlewanger
Delphine Huser
Eric Girardin
September 2011
0 references