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  PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)

Bergmann, C., Senderek, J., Schneider, F., Dornia, C., Kupper, F., Eggermann, T., et al. (2004). PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD). Human Mutation, 23(5), 487-495.

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Genre: Journal Article
Alternative Title : Hum. Mutat.

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 Creators:
Bergmann, C., Author
Senderek, J., Author
Schneider, F., Author
Dornia, C., Author
Kupper, F., Author
Eggermann, T., Author
Rudnik-Schöneborn, S., Author
Kirfel, J., Author
Moser, M.1, Author           
Büttner, R., Author
Zerres, K., Author
Affiliations:
1Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565147              

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Free keywords: autosomal recessive polycystic kidney disease; ARPKD; polycystic kidney and hepatic disease 1; PKHD1; fibrocystin; polyductin; mutation analysis; genotype-phenotype correlation; prenatal diagnosis
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Language(s): eng - English
 Dates: 2004
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 221576
ISI: 000221119500012
 Degree: -

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Title: Human Mutation
  Alternative Title : Hum. Mutat.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 23 (5) Sequence Number: - Start / End Page: 487 - 495 Identifier: ISSN: 1059-7794