Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Siri L Rydning"'
Autor:
Zafar Iqbal, Siri L Rydning, Iselin M Wedding, Jeanette Koht, Lasse Pihlstrøm, Aina H Rengmark, Sandra P Henriksen, Chantal M E Tallaksen, Mathias Toft
Publikováno v:
PLoS ONE, Vol 12, Iss 3, p e0174667 (2017)
Hereditary ataxia and spastic paraplegia are heterogeneous monogenic neurodegenerative disorders. To date, a large number of individuals with such disorders remain undiagnosed. Here, we have assessed molecular diagnosis by gene panel sequencing in 10
Externí odkaz:
https://doaj.org/article/9a3d5f8bc6bf4856be877bc902e467dc
Autor:
Zafar Iqbal, Siri L Rydning, Iselin M Wedding, Jeanette Koht, Lasse Pihlstrøm, Aina H Rengmark, Sandra P Henriksen, Chantal M E Tallaksen, Mathias Toft
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186571 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0174667.].
Externí odkaz:
https://doaj.org/article/68446d3120a34f73ada9029a2bab7aa7