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X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males
- Jais, JP (author)
- Knebelmann, B (author)
- Giatras, I (author)
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- De Marchi, M (author)
- Rizzoni, G (author)
- Renieri, A (author)
- Weber, M (author)
- Gross, O (author)
- Netzer, KO (author)
- Flinter, F (author)
- Pirson, Y (author)
- Verellen, C (author)
- Wieslander, J (author)
- Persson, U (author)
- Martin, P (author)
- Hertz, JM (author)
- Schroder, C (author)
- Sanak, M (author)
- Krejcova, S (author)
- Carvalho, MF (author)
- Saus, J (author)
- Antignac, C (author)
- Smeets, H (author)
- Gubler, MC (author)
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- (creator_code:org_t)
- 2000
- 2000
- English.
- In: Journal of the American Society of Nephrology : JASN. - 1046-6673. ; 11:4, s. 649-657
- Journal article (peer-reviewed)
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- Jais, JP
- Knebelmann, B
- Giatras, I
- De Marchi, M
- Rizzoni, G
- Renieri, A
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- Weber, M
- Gross, O
- Netzer, KO
- Flinter, F
- Pirson, Y
- Verellen, C
- Wieslander, J
- Persson, U
- Tryggvason, K
- Martin, P
- Hertz, JM
- Schroder, C
- Sanak, M
- Krejcova, S
- Carvalho, MF
- Saus, J
- Antignac, C
- Smeets, H
- Gubler, MC
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- Karolinska Institutet
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