Cite
HARVARD Citation
Sakoh, T. et al. (2019). A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4. Molecular genetics & genomic medicine. 7 (6), p. n/a. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Sakoh, T. et al. (2019). A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4. Molecular genetics & genomic medicine. 7 (6), p. n/a. [Online].