MKS3-Related Ciliopathy with Features of Autosomal Recessive Polycystic Kidney Disease, Nephronophthisis, and Joubert Syndrome-Reference-Cited by-同舟云学术

MKS3-Related Ciliopathy with Features of Autosomal Recessive Polycystic Kidney Disease, Nephronophthisis, and Joubert Syndrome

Published:2009-09 Issue:3 Volume:155 Page:386-392.e1
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Gunay-Aygun Meral,Parisi Melissa A.,Doherty Dan,Tuchman Maya,Tsilou Ekaterini,Kleiner David E.,Huizing Marjan,Turkbey Baris,Choyke Peter,Guay-Woodford Lisa,Heller Theo,Szymanska Katarzyna,Johnson Colin A.,Glass Ian,Gahl William A.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference26 articles.

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4. Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft fur Padiatrische, Nephrologie;Zerres;Acta Paediatr,1996

5. PKHD1, the polycystic kidney and hepatic disease 1 gene, encodes a novel large protein containing multiple immunoglobulin-like plexin-transcription-factor domains and parallel beta-helix 1 repeats;Onuchic;Am J Hum Genet,2002

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