Homozygous missense mutation in SLC 12A3 gene caused Gitelmanś syndrome with chondrocalcinosis | Charles Explorer

Homozygous missense mutation in SLC 12A3 gene caused Gitelmanś syndrome with chondrocalcinosis

Publikace

Abstrakt

Gitelmanś syndrome, SLC12A3 gene, chondrocalcinosis

Osoby