Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder (Q41694710)
Jump to navigation
Jump to search
scientific article published on 11 December 2014
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder |
scientific article published on 11 December 2014 |
Statements
1 reference
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder (English)
1 reference
Nienke Wieskamp
Raman Kumar
Mark A Corbett
Nicholas J C Smith
Chuan Tan
Michael D Duffield
Toshihiko Utsumi
Koko Moriya
Katherine R Smith
Kim Abbott
Joshua A Woenig
Sabine Gijsen
Melanie Bahlo
Joseph G Gleeson
Eric Haan
Alexander Hoischen
11 December 2014
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference