Missense mutations in DYT-TOR1A dystonia

por Iqbal, Zafar, Koht, Jeanette, Pihlstrøm, Lasse, Henriksen, Sandra P., Cappelletti, Chiara, Russel, Michael Bjørn, Norberto de Souza, Osmar, Skogseid, Inger Marie, Toft, Mathias
Publicado 2019

Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

por Iqbal, Zafar, Rydning, Siri L., Wedding, Iselin M., Koht, Jeanette, Pihlstrøm, Lasse, Rengmark, Aina H., Henriksen, Sandra P., Tallaksen, Chantal M. E., Toft, Mathias
Publicado 2017

Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

por Iqbal, Zafar, Rydning, Siri L., Wedding, Iselin M., Koht, Jeanette, Pihlstrøm, Lasse, Rengmark, Aina H., Henriksen, Sandra P., Tallaksen, Chantal M. E., Toft, Mathias
Publicado 2017