Homozygous Missense Mutation on Exon 22 of PKHD1 Gene Causing Fatal Autosomal Recessive Polycystic Kidney Disease
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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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
- Beteiligte Personen und Organisationen
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Sathyan, Sajina
Pournami, Femitha
Madhavilatha, Gopala Krishna
Tuteja, Amrit
Nandakumar, Anand
Prabhakar, Jyothi
Jain, Naveen
- DOI
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10.1055/s-0041-1725175
- URN
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urn:nbn:de:101:1-2021060411405878316077
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:45 MESZ
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Beteiligte
- Sathyan, Sajina
- Pournami, Femitha
- Madhavilatha, Gopala Krishna
- Tuteja, Amrit
- Nandakumar, Anand
- Prabhakar, Jyothi
- Jain, Naveen
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