INVESTIGACIÓN EN ENFERMEDADES RARAS
Necker-Enfants Malades Hospital
París, FranciaPublications en collaboration avec des chercheurs de Necker-Enfants Malades Hospital (2)
2012
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PRKAR1A and PDE4D mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance
Journal of Clinical Endocrinology and Metabolism, Vol. 97, Núm. 12
2007
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New ABCC8 mutations in relapsing neonatal diabetes and clinical features
Diabetes, Vol. 56, Núm. 6, pp. 1737-1741