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
Undiagnosed Dis Network
Scottish Genome Partnership
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