Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen
Zerres, K. ; Mücher, G. ; Bachner, L. ; Deschennes, G. ; Eggermann, T. ; Kääriäinen, H. ; Knapp, M. ; Lennert, T. ; Misselwitz, J. ; von Mühlendahl, K. E. ; Neumann, H. P. H. ; Pirson, Y. ; Rudnik-Schöneborn, S. ; Steinbicker, V. ; Wirth, B. ; Schärer, K.
[s.l.] : Nature Publishing Group
Published 1994
[s.l.] : Nature Publishing Group
Published 1994
ISSN: |
1546-1718
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Source: |
Nature Archives 1869 - 2009
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Topics: |
Biology
Medicine
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Notes: |
[Auszug] Autosomal recessive polycystic kidney disease (ARPKD) is one of the major hereditary nephropathies in children predominantly presenting in early childhood. The clinical picture is variable but there is a fatal outcome in many cases. We have performed linkage analysis in 16 ARPKD families and ...
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Type of Medium: |
Electronic Resource
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URL: |