E. Also

Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene

Laura Alías, Sara Bernal, Pablo Fuentes‐Prior et al. · Human Genetics · 2008 · 169 citations

Life Sciences, Genetics, Molecular Genetics +13

The Developmental Pattern of Myotubes in Spinal Muscular Atrophy Indicates Prenatal Delay of Muscle Maturation

Rebeca Martínez‐Hernández, Carolina Soler‐Botija, E. Also et al. · Journal of Neuropathology & Experimental Neurology · 2009 · 102 citations

Medicine, Neurobiology, Neuroscience +17

Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population

Mandana Hasanzad, Maryam Azad, Kimia Kahrizi et al. · European Journal of Neurology · 2009 · 32 citations

Life Sciences, Genetics, Molecular Genetics +15

Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: Clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients

Josep Gámez, E. Also, Laura Alías et al. · Clinical Neurology and Neurosurgery · 2007 · 15 citations

Life Sciences, Genetics, Molecular Genetics +13