Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease ; volume:11 ; number:01 ; year:2021 ; pages:e70-e73
Journal of child science ; 11, Heft 01 (2021), e70-e73

Contributor
Sathyan, Sajina
Pournami, Femitha
Madhavilatha, Gopala Krishna
Tuteja, Amrit
Nandakumar, Anand
Prabhakar, Jyothi
Jain, Naveen

DOI
10.1055/s-0041-1725175
URN
urn:nbn:de:101:1-2021060411405878316077
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:45 AM CEST

Data provider

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Associated

  • Sathyan, Sajina
  • Pournami, Femitha
  • Madhavilatha, Gopala Krishna
  • Tuteja, Amrit
  • Nandakumar, Anand
  • Prabhakar, Jyothi
  • Jain, Naveen

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