Molecular modeling of disease causing mutations in domain C1 of cMyBP-C.

by Poornima Gajendrarao, Navaneethakrishnan Krishnamoorthy, Heba Sh Kassem, Sarah Moharem-Elgamal, Franco Cecchi, Iacopo Olivotto, Magdi H Yacoub
Published 2013-01-01

Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy N...

by Anna Morgan, Stefania Lenarduzzi, Stefania Cappellani, Vanna Pecile, Marcello Morgutti, Eva Orzan, Sara Ghiselli, Umberto Ambrosetti, Marco Brumat, Poornima Gajendrarao, Martina La Bianca, Flavio Faletra, Enrico Grosso, Fabio Sirchia, Alberto Sensi, Claudio Graziano, Marco Seri, Paolo Gasparini, Paolo Gasparini, Giorgia Girotto, Giorgia Girotto
Published 2018-12-01