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Figure 1 | BMC Urology

Figure 1

From: A rare case of unilateral adrenal hyperplasia accompanied by hypokalaemic periodic paralysis caused by a novel dominant mutation in CACNA1S: features and prognosis after adrenalectomy

Figure 1

Mutation Detection of CACNA1S in the Family of Hypokalaemic Periodic Paralysis, Type I (HOKPP1). Panel A shows the family pedigree with the patient as the proband (arrow). Panel B shows the DNA sequencing results of CACNA1S of the patient and a healthy control and the position of the c.1582C > T heterozygous mutation (arrow). The mutation leads to an amino acid substitution of Arg for Cys at the 528th codon of CACNA1S.

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BMC Urology

ISSN: 1471-2490

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