Skip to main content
Fig. 2 | BMC Pediatrics

Fig. 2

From: Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report

Fig. 2

Sequencing of the NPHP1 gene. a DNA sequencing profile showing exon8 c.922 T > C (p.Ser308Pro) in NPHP1, which was derived from the patient’s mother. The arrow indicates the position of the mutation. b The exon 17 c.1757G > A (p.Arg586Gln) mutation in NPHP1 was inherited from the patient’s father. The arrow indicates the position of the mutation

Back to article page

BMC Pediatrics

ISSN: 1471-2431

Contact us