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6. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
作者：Crystel Bonnet (1) (2)
M’hamed Grati (1) (2) (30)
Sandrine Marlin (1)
Jacqueline Levilliers (2)
Jean-Pierre Hardelin (2)
Marine Parodi (3)
Magali Niasme-Grare (3)
Diana Zelenika (4)
Marc Délépine (4)
Delphine Feldmann (1) (3)
Laurence Jonard (1) (3)
Aziz El-Amraoui (2)
Dominique Weil (2)
Bruno Delobel (5)
Christophe Vincent (6)
Hélène Dollfus (7)
Marie-Madeleine Eliot (8)
Albert David (9)
Catherine Calais (10)
Jacqueline Vigneron (11)
Bettina Montaut-Verient (12)
Dominique Bonneau (13)
Jacques Dubin (14)
Christel Thauvin (15)
Alain Duvillard (16)
Christine Francannet (17)
Thierry Mom (18)
Didier Lacombe (19)
Fran?oise Duriez (20)
Valérie Drouin-Garraud (21)
Marie-Fran?oise Thuillier-Obstoy (22)
Sabine Sigaudy (23)
Anne-Marie Frances (24)
Patrick Collignon (24)
Georges Challe (25)
Rémy Couderc (1) (3)
Mark Lathrop (4)
José-Alain Sahel (26)
Jean Weissenbach (27)
Christine Petit (2) (28)
Fran?oise Denoyelle (2) (29)
刊名：Orphanet Journal of Rare Diseases
出版年：2011
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