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X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study

AuthID
P-000-F15

Author(s)

Jais, JP

Knebelmann, B

Giatras, I

De Marchi, M

Rizzoni, G

Renieri, A

Weber, M

Gross, O

Netzer, KO

Flinter, F

[+4]·

Tryggvason, K

Martin, P

Hertz, JM

Schroder, C

Sanak, M

Carvalho, MF

Saus, J

Antignac, C

Smeets, H

Gubler, MC

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Tipo de Documento

Article

Year published

2003

Publicado

in JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, ISSN: 1046-6673

Volume: 14, Número: 10, Páginas: 2603-2610 (8)

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Publication Identifiers

DOI: 10.1097/01.asn.0000090034.71205.74

Pubmed: 14514738

SCOPUS: 2-s2.0-0141566829

Wos: WOS:000185540800022

Source Identifiers

ISSN: 1046-6673

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All authors

Name Order	Nome	Name Order	Nome	Name Order	Nome
1	Jais, JP;	2	Knebelmann, B;	3	Giatras, I;
4	De Marchi, M;	5	Rizzoni, G;	6	Renieri, A;
7	Weber, M;	8	Gross, O;	9	Netzer, KO;
10	Flinter, F;	11	Pirson, Y;	12	Dahan, K;
13	Wieslander, J;	14	Persson, U;	15	Tryggvason, K;
16	Martin, P;	17	Hertz, JM;	18	Schroder, C;
19	Sanak, M;	20	Carvalho, MF;	21	Saus, J;
22	Antignac, C;	23	Smeets, H;	24	Gubler, MC;

X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study

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X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A "European Community Alport Syndrome Concerted Action" Study

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