Fig. 2
From: A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia
Sequences of the patient, her children and her father. The above sequence column is the reference sequence, next are the sequence of the patient and her son, daughter, father, respectively. The columns below tested sequences are subtracted results of tested sequence and reference sequence, which show homozygous c.2039delG of the patient and heterozygous mutation of her children and father)