Behzad Moghadaszadeh

Directed evolution of a family of AAV capsid variants enabling potent muscle-directed gene delivery across species

Mohammadsharif Tabebordbar, Kim A. Lagerborg, Alexandra C. Stanton et al. · Cell · 2021 · 465 citations · Full text

Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome

Behzad Moghadaszadeh, Nathalie Petit, Céline Jaillard et al. · Nature Genetics · 2001 · 364 citations

Rare Diseases, Developmental Biology, Mendelian Disorder +9

Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies

Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau et al. · The American Journal of Human Genetics · 2002 · 361 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Classical Phenotype +9

Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1)

Eugenio Mercuri, Beril Talim, Behzad Moghadaszadeh et al. · Neuromuscular Disorders · 2002 · 213 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +5

Mutations in COL6A3 Cause Severe and Mild Phenotypes of Ullrich Congenital Muscular Dystrophy

Ercan Demir, Patrizia Sabatelli, Valérie Allamand et al. · The American Journal of Human Genetics · 2002 · 167 citations · Full text

Rare Diseases, Mendelian Disorder, Genetic Disorder +9