1
ERRATUM Erratum to: Bilineal inheritance of PKD1 abnormalities mimicking autosomal recessive polycystic disease Rodney D. Gilbert & Priya Sukhtankar & Katherine Lachlan & Darren J. Fowler Published online: 9 August 2013 # IPNA 2013 Erratum to: Pediatr Nephrol DOI 10.1007/s00467-013-2484-x Two errors appeared in the Abstract, in the paragraph Conclusion. The correct text should be: Biallelic inheritance of abnormalities of PKD1 may cause extremely severe disease resembling autosomal recessive polycystic kidney disease (ARPKD) which can result in diagnostic confusion. Accurate diagnosis is essential for genetic counseling The online version of the original article can be found at http://dx.doi.org/ 10.1007/s00467-013-2484-x. R. D. Gilbert (*) : P. Sukhtankar Regional Paediatric Nephro-Urology Unit, University Hospital Southampton, Tremona Road, Southampton SO16 6YD, UK e-mail: [email protected] R. D. Gilbert : P. Sukhtankar School of Medicine, University of Southampton, Southampton, UK K. Lachlan Wessex Clinical Genetics Service, University Hospital Southampton, Southampton, UK K. Lachlan Human Genetics & Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK D. J. Fowler Cell Pathology Department, University Hospital Southampton, Tremona Road, Southampton, UK Pediatr Nephrol (2013) 28:2233 DOI 10.1007/s00467-013-2508-6

Erratum to: Bilineal inheritance of PKD1 abnormalities mimicking autosomal recessive polycystic disease

Embed Size (px)

Citation preview

Page 1: Erratum to: Bilineal inheritance of PKD1 abnormalities mimicking autosomal recessive polycystic disease

ERRATUM

Erratum to: Bilineal inheritance of PKD1 abnormalitiesmimicking autosomal recessive polycystic disease

Rodney D. Gilbert & Priya Sukhtankar &

Katherine Lachlan & Darren J. Fowler

Published online: 9 August 2013# IPNA 2013

Erratum to: Pediatr NephrolDOI 10.1007/s00467-013-2484-x

Two errors appeared in the Abstract, in the paragraphConclusion.

The correct text should be:Biallelic inheritance of abnormalities of PKD1 may cause

extremely severe disease resembling autosomal recessivepolycystic kidney disease (ARPKD) which can result indiagnostic confusion. Accurate diagnosis is essential forgenetic counseling

The online version of the original article can be found at http://dx.doi.org/10.1007/s00467-013-2484-x.

R. D. Gilbert (*) : P. SukhtankarRegional Paediatric Nephro-Urology Unit,University Hospital Southampton, Tremona Road,Southampton SO16 6YD, UKe-mail: [email protected]

R. D. Gilbert : P. SukhtankarSchool of Medicine, University of Southampton,Southampton, UK

K. LachlanWessex Clinical Genetics Service, University HospitalSouthampton, Southampton, UK

K. LachlanHuman Genetics & Genomic Medicine, Faculty of Medicine,University of Southampton, Southampton, UK

D. J. FowlerCell Pathology Department, University Hospital Southampton,Tremona Road,Southampton, UK

Pediatr Nephrol (2013) 28:2233DOI 10.1007/s00467-013-2508-6