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Homozygous Missense Variants in NTNG2, Encoding a Presynapt..:

Dias, CM ; Punetha, J ; Zheng, C...
https://discovery.ucl.ac.uk/id/eprint/10085720/1/Houlden_Homozygous%20Missense%20Variants%20in%20NTNG2_VoR.pdf. , 2019

Link: https://discovery.ucl.ac.uk/id/eprint/10085720/1/Hould..

RT Journal
T1 <Title>Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10085720&Exemplar=1&LAN=DE
				
A1 Dias, CM
A1 Punetha, J
A1 Zheng, C
A1 Mazaheri, N
A1 Rad, A
A1 Efthymiou, S
A1 Petersen, A
A1 Dehghani, M
A1 Pehlivan, D
A1 Partlow, JN
A1 Posey, JE
A1 Salpietro, V
A1 Gezdirici, A
A1 Malamiri, RA
A1 Al Menabawy, NM
A1 Selim, LA
A1 Vahidi Mehrjardi, MY
A1 Banu, S
A1 Polla, DL
A1 Yang, E
A1 Rezazadeh Varaghchi, J
A1 Mitani, T
A1 van Beusekom, E
A1 Najafi, M
A1 Sedaghat, A
A1 Keller-Ramey, J
A1 Durham, L
A1 Coban-Akdemir, Z
A1 Karaca, E
A1 Orlova, V
A1 Schaeken, LLM
A1 Sherafat, A
A1 Jhangiani, SN
A1 Stanley, V
A1 Shariati, G
A1 Galehdari, H
A1 Gleeson, JG
A1 Walsh, CA
A1 Lupski, JR
A1 Seiradake, E
A1 Houlden, H
A1 van Bokhoven, H
A1 Maroofian, R
YR 2019
K1 NTNG2
K1 autism
K1 developmental delay
K1 intellectual disability
K1 neurodevelopmental disorder
JF https://discovery.ucl.ac.uk/id/eprint/10085720/1/Houlden_Homozygous%20Missense%20Variants%20in%20NTNG2_VoR.pdf
LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10085720/1/Houlden_Homozygous%20Missense%20Variants%20in%20NTNG2_VoR.pdf
DO https://discovery.ucl.ac.uk/id/eprint/10085720/1/Houlden_Homozygous%20Missense%20Variants%20in%20NTNG2_VoR.pdf
SF ELIB - SuUB Bremen

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