Enfermedades Raras y Medicina Pediátrica
Venetian Institute of Molecular Medicine
Padua, ItaliaPublicaciones en colaboración con investigadores/as de Venetian Institute of Molecular Medicine (2)
2010
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The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice
Journal of Biological Chemistry, Vol. 285, Núm. 48, pp. 37693-37703
2007
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A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness
Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Núm. 5, pp. 1516-1521