Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early‐onset and fast cyst progression-Reference-Cited by-同舟云学术

Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early‐onset and fast cyst progression

Published:2020-03-25 Issue:6 Volume:97 Page:857-868
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Peces Ramón¹^ORCID,Mena Rocio²,Peces Carlos³,Cuesta Emilio⁴,Selgas Rafael¹,Barruz Pilar²,Lapunzina Pablo²⁵^ORCID,Nevado Julián²⁵

Affiliation:

1. Servicio de Nefrología, Hospital Universitario La Paz, IdiPAZUniversidad Autonoma Madrid Spain

2. Instituto de Genética Médica y Molecular (INGEMM)‐IdiPAZ, Hospital Universitario La PazUniversidad Autonoma Madrid Spain

3. Area de Tecnología de la Información, SESCAM Toledo Spain

4. Servicio de Radiología, Hospital Universitario La Paz, IdiPAZUniversidad Autonoma Madrid Spain

5. CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII Madrid Spain

Funder

Ministerio de Ciencia e Innovación

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13738

Reference51 articles.

1. Type of PKD1 Mutation Influences Renal Outcome in ADPKD

2. Genetic Complexity of Autosomal Dominant Polycystic Kidney and Liver Diseases

3. Polycystic kidney disease

4. Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

5. Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease

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