Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Identification of TAZ mutations in pediatric patients with cardiomyopathy by targeted next-generation sequencing in a Chinese cohort

Fig. 1

Sanger sequencing chromatograms. a Novel TAZ mutation c.527A > G (p.H176R) in proband 1: (top) Hemizygous mutation for the proband; (middle) Heterozygous mutation for the proband’s mother; (bottom) Hemizygous normal allele for the proband’s father. b Novel TAZ mutation c.134_136delinsCC (p.H45PfsX38) in proband 4: (top) Hemizygous mutation for the proband; (middle) Heterozygous mutation for the proband’s mother; (bottom) Hemizygous normal allele for the proband’s father

Back to article page

Orphanet Journal of Rare Diseases

ISSN: 1750-1172