Complex disease phenotype revealed by GH deficiency associated with a novel and unusual defect in the GH-1 gene

Authors: Iughetti, Lorenzo¹; Sobrier, Marie-Laure²; Predieri, Barbara¹; Netchine, Irene²; Carani, Cesare³; Bernasconi, Sergio¹; Balli, Fiorella¹; Amselem, Serge²

Source: Clinical Endocrinology, Volume 69, Number 1, July 2008 , pp. 170-172(3)

Publisher: Wiley-Blackwell

Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1365-2265.2007.03157.x

Affiliations: 1: Departments of Paediatrics and 2: INSERM U654, Hôpital Armand-Trousseau, Paris 75012, France, Email: iughetti.lorenzo@unimore.it 3: Endocrinology, Universities of Modena and Reggio Emilia, and Parma, Italy and

Publication date: 2008-07-01

• In this: publication
• By this: publisher
• In this Subject: Anatomy & Physiology ,  Internal Medicine
• By this author: Iughetti, Lorenzo ;  Sobrier, Marie-Laure ;  Predieri, Barbara ;  Netchine, Irene ;  Carani, Cesare ;  Bernasconi, Sergio ;  Balli, Fiorella ;  Amselem, Serge

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