Title: | New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes |
Journal : | Neurology. Genetics, 6, 6 |
Authors: | Bauche S ; Sureau A ; Sternberg D ; Rendu J ; Buon C ; Messéant J ; Boex M ; Furling D ; Fauré J ; Latypova X ; Gelot AB ; Mayer M ; Mary P ; Whalen S ; Fournier E ; Cloix I ; Remerand G ; Laffargue F ; Nougues MC ; Fontaine B ; Eymard B ; Isapof A ; Strochlic L |
Material Type: | Article |
Publication Date: | 03/12/2020 |
Size: | p e534 |
Languages: | English |
Pubmed / DOI : | Pubmed : 33659639 / DOI : 10.1212/NXG.0000000000000534 |
N° Profil MNM : | 2021031 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/33659639 |