Alix de Becdelièvre

Heterogeneity of lung disease associated with NK2 homeobox 1 mutations

Elodie Nattes, Stéphanie Lejeune, A. Carsin et al. · Respiratory Medicine · 2017 · 86 citations

Nk2 Homeobox 1, Immunology, Pathology +5

New syndromic form of benign hereditary chorea is associated with a deletion of TITF‐1 and PAX‐9 contiguous genes

David Devos, Isabelle Vuillaume, Alix de Becdelièvre et al. · Movement Disorders · 2006 · 76 citations

Correlation between <i>PABPN1</i> genotype and disease severity in oculopharyngeal muscular dystrophy

Pascale Richard, Capucine Trollet, Tanya Stojkovic et al. · Neurology · 2016 · 70 citations · Full text

Alternative Splicing at a NAGNAG Acceptor Site as a Novel Phenotype Modifier

Alexandre Hinzpeter, Abdel Aissat, Elvira Sondo et al. · PLoS Genetics · 2010 · 65 citations · Full text

Nagnag Acceptor Site, Genetics, Rna Splicing +18

COMMD1-Mediated Ubiquitination Regulates CFTR Trafficking

Loïc Drévillon, Gaëlle Tanguy, Alexandre Hinzpeter et al. · PLoS ONE · 2011 · 51 citations · Full text

Molecular Physiology, Signal Transduction, Cftr Processing +14