PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity

Author: Monnier Carine   Dod Catherine   Fabre Ludovic   Teixeira Luis   Labesse Gilles   Pin Jean-Philippe   Hardelin Jean-Pierre   Rondard Philippe  

Publisher: Oxford University Press

E-ISSN: 0964-6906|18|1|75-81

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.18, Iss.1, 2009-01, pp. : 75-81

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