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Publication date
2018 10 04
Authors
Ferreira, CR Xia, ZJ Clement, A Parry, DA Davids, M Taylan, F Sharma, P Turgeon, CT Blanco-Sanchez, B Ng, BG Logan, CV Wolfe, LA Solomon, BD Cho, MT Douglas, G Carvalho, DR Bratke, H Haug, MG Phillips, JB Wegner, J Tiemeyer, M Aoki, K Nordgren, A Hammarsjo, A Duker, AL Rohena, L Hove, HB Ek, J Adams, D Tifft, CJ Onyekweli, T Weixel, T Macnamara, E Radtke, K Powis, Z Earl, D Gabriel, M Russi, AHS Brick, L Kozenko, M Tham, E Raymond, KM Phillips, JA Tiller, GE Wilson, WG Hamid, R Malicdan, MCV Nishimura, G Grigelioniene, G Jackson, A Westerfield, M Bober, MB Gahl, WA Freeze, HH
Group authors
Scottish Genome Partnership Undiagnosed Dis Network
Author KI Usernames
Grigelioniene, G|giegri Hammarsjo, A|annaha3 Hammarsjö, A|annaha3 Nordgren, A|annord Taylan, F|fultay Tham, E|emmcar
Pubmed ID
30290151
Journal
American journal of human genetics
Doctype
Article
KI Connection
Medel
Mesh SV
Aminosyrasubstitution Barn Cellinje Djur Endoplasmatiskt nätverk Extracellulär matrix Fibroblaster Fragil X-syndrom Förskolebarn Genmanipulerade djur Glykosylering Golgiapparat Heterozygot Kvinnlig Manlig Människa Proteintransport Proteoglykaner Sebrafisk Spädbarn Vesikulära transportproteiner Vuxna
Mesh EN
Amino Acid Substitution Animals, Genetically Modified Cell Line Endoplasmic Reticulum Extracellular Matrix Fibroblasts Fragile X Syndrome Glycosylation Golgi Apparatus Heterozygote Protein Transport Proteoglycans Vesicular Transport Proteins Zebrafish
First date
2018-10-21T23:41:19.571Z