HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Pediatric nephrology (Berlin, West)

• Publication date

  2011-03-05

• Fields of study

  Medicine

• Identifiers
  DOI 10.1007/s00467-011-1826-9PMID 21380624PMCID PMC3257470
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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