[Retracted] A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation

Table 2

Analysis of the X-chromosome inactivation pattern in the family.

	Subjects
	II-3	II-4	III-3	III-4	III -7
Fragment length allele 1 (bp)	280	280	280	280	280
Fragment length allele 2 (bp)	292	292	292	292	292
Percentage of cells with allele 1 as inactive X-chromosome (%)	90	83	87	85	39
Percentage of cells with allele 2 as inactive X-chromosome (%)	10	17	13	15	61