Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé; Luis Teixeira; Jacqueline Levilliers; Corinne Fouveaut; Philippe Bouchard; Marie-Laure Kottler; James Lespinasse; Anne Lienhardt-Roussie; Michèle Mathieu; Alexandre Moerman; Graeme Morgan; Arnaud Murat; Jean-Edmont Toublanc; Slawomir Wolczynski; Marc Delpech; Christine Petit; Jacques Young; Jean-Pierre Hardelin

doi:10.1371/journal.pgen.0020175

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Peer-reviewed

Research Article

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé ,

*To whom correspondence should be addressed. E-mail: dode@cochin.inserm.fr (CD), hardelin@pasteur.fr (JPH)

Affiliation Institut Cochin, INSERM U567, Université René Descartes, Paris, France
⨯
Luis Teixeira,

Affiliation Institut Cochin, INSERM U567, Université René Descartes, Paris, France
⨯
Jacqueline Levilliers,

Affiliation Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut Pasteur, Paris, France
⨯
Corinne Fouveaut,

Affiliation Laboratoire de Biochimie Génétique, Hôpital Cochin, Paris, France
⨯
Philippe Bouchard,

Affiliation Service d'Endocrinologie, Hôpital Saint-Antoine, Paris, France
⨯
Marie-Laure Kottler,

Affiliation Service de Génétique, Centre Hospitalier, Caen, France
⨯
James Lespinasse,

Affiliation Laboratoire de Génétique Chromosomique, Centre Hospitalier, Chambéry, France
⨯
Anne Lienhardt-Roussie,

Affiliation Service d'Endocrinologie Pédiatrique, CHU Dupuytren, Limoges, France
⨯
Michèle Mathieu,

Affiliation Département de Pédiatrie, Centre Hospitalier, Amiens, France
⨯
Alexandre Moerman,

Affiliation Service de Génétique, Hôpital Jeanne de Flandres, Lille, France
⨯
Graeme Morgan,

Affiliation Sydney IVF, Sydney, Australia
⨯
Arnaud Murat,

Affiliation Clinique d'Endocrinologie, Maladies Métaboliques et Nutrition, Hôtel-Dieu, Nantes, France
⨯
Jean-Edmont Toublanc,

Affiliation Service d'Endocrinologie Pédiatrique, Hôpital Saint-Vincent de Paul, Paris, France
⨯
Slawomir Wolczynski,

Affiliation Department of Reproduction and Gynecological Endocrinology, Bialystok, Poland
⨯
Marc Delpech,

Affiliation Institut Cochin, INSERM U567, Université René Descartes, Paris, France
⨯
Christine Petit,

Affiliation Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut Pasteur, Paris, France
⨯
Jacques Young,

Affiliation Service d'Endocrinologie, Hôpital de Bicêtre, Le Kremlin-Bicêtre, France
⨯
[ ... ],
Jean-Pierre Hardelin

*To whom correspondence should be addressed. E-mail: dode@cochin.inserm.fr (CD), hardelin@pasteur.fr (JPH)

Affiliation Unité de Génétique des Déficits Sensoriels, INSERM U587, Institut Pasteur, Paris, France
⨯
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Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

Catherine Dodé,
Luis Teixeira,
Jacqueline Levilliers,
Corinne Fouveaut,
Philippe Bouchard,
Marie-Laure Kottler,
James Lespinasse,
Anne Lienhardt-Roussie,
Michèle Mathieu,
Alexandre Moerman

Published: October 20, 2006
https://doi.org/10.1371/journal.pgen.0020175

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30 May 2008
11:24 GMT
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Publisher's Note: Correction to Nomenclature in Table 1, Figure 1, and Figure S1 Posted by PLOS_Genetics on 30 May 2008 at 11:24 GMT

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