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

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis

por Rydning, Siri L, Koht, Jeanette, Sheng, Ying, Sowa, Piotr, Hjorthaug, Hanne S, Wedding, Iselin M, Erichsen, Anne Kjersti, Hovden, Inger Anette, Backe, Paul H, Tallaksen, Chantal M E, Vigeland, Magnus D, Selmer, Kaja K
Publicado 2019