Case Report: Compound Heterozygous SCNN1B Mutations Causing Pseudohypoaldosteronism Type 1B2 in Neonatal Twins.

Wang Z, Long L, Bi H

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DOI: 10.1002/mgg3.70173
Published: 2026 Jan
Container: Molecular genetics & genomic medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/mgg3.70173,
  title = {Case Report: Compound Heterozygous SCNN1B Mutations Causing Pseudohypoaldosteronism Type 1B2 in Neonatal Twins.},
  author = {Wang Z and Long L and Bi H},
  year = {2026},
  journal = {Molecular genetics \& genomic medicine},
  doi = {10.1002/mgg3.70173},
  url = {https://doi.org/10.1002/mgg3.70173}
}

RIS

TY  - JOUR
TI  - Case Report: Compound Heterozygous SCNN1B Mutations Causing Pseudohypoaldosteronism Type 1B2 in Neonatal Twins.
AU  - Wang Z
AU  - Long L
AU  - Bi H
PY  - 2026
JO  - Molecular genetics & genomic medicine
DO  - 10.1002/mgg3.70173
UR  - https://doi.org/10.1002/mgg3.70173
ER  -

APA

Z, W., L, L., & H, B. (2026). Case Report: Compound Heterozygous SCNN1B Mutations Causing Pseudohypoaldosteronism Type 1B2 in Neonatal Twins.. Molecular genetics & genomic medicine. https://doi.org/10.1002/mgg3.70173

Source records

pubmed · retrieved 2026-09-26T19:53:13.032Z
europe-pmc · retrieved 2026-09-26T19:53:13.039Z
doaj · retrieved 2026-09-26T19:53:13.034Z