We report a second founder mutation among GS patients of Roma ethnic background. The direct screening of this mutation would facilitate the characterization of patients who are negative for the more common intron 9 +1G>T mutation.
Antecedentes genéticos en etnia gitana; Gen SLC12A3; Gitelman's syndrome; Gypsy patients; Pacientes de Roma background; SLC12A3 gene; Síndrome de Gitelman
