APA

Richard P., Trollet C., Gidaro T., Demay L., Brochier G., Malfatti E., Tom F. M., Fardeau M., Lafor P., Romero N., Martin-N M., Sol G., Ferrer-Monasterio X., Saint-Guily J. L. & Eymard B. (2015). PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling. : Journal of neuromuscular diseases.

Chicago

Richard Pascale, Trollet Capucine, Gidaro Teresa, Demay Laurence, Brochier Guy, Malfatti Edoardo, Tom Fernando Ms, Fardeau Michel, Lafor Pascal, Romero Norma, Martin-N Marie-Laure, Sol Guilhem, Ferrer-Monasterio Xavier, Saint-Guily Jean Lacau and Eymard Bruno. 2015. PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling. : Journal of neuromuscular diseases.

Harvard

Richard P., Trollet C., Gidaro T., Demay L., Brochier G., Malfatti E., Tom F. M., Fardeau M., Lafor P., Romero N., Martin-N M., Sol G., Ferrer-Monasterio X., Saint-Guily J. L. and Eymard B. (2015). PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling. : Journal of neuromuscular diseases.

MLA

Richard Pascale, Trollet Capucine, Gidaro Teresa, Demay Laurence, Brochier Guy, Malfatti Edoardo, Tom Fernando Ms, Fardeau Michel, Lafor Pascal, Romero Norma, Martin-N Marie-Laure, Sol Guilhem, Ferrer-Monasterio Xavier, Saint-Guily Jean Lacau and Eymard Bruno. PABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling. : Journal of neuromuscular diseases. 2015.