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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodev..:

O'Donnell-Luria, AH ; Pais, LS ; Faundes, V...
https://openaccess.sgul.ac.uk/id/eprint/113838/1/O%27Donnell-LuriaetalAAM2019.pdf. , 2019

Link: https://openaccess.sgul.ac.uk/id/eprint/113838/

RT Journal
T1 <Title>Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftstgeorgesuniv:oai:openaccess.sgul.ac.uk:113838&Exemplar=1&LAN=DE
				
A1 O'Donnell-Luria, AH
A1 Pais, LS
A1 Faundes, V
A1 Wood, JC
A1 Sveden, A
A1 Luria, V
A1 Abou Jamra, R
A1 Accogli, A
A1 Amburgey, K
A1 Anderlid, BM
A1 Azzarello-Burri, S
A1 Basinger, AA
A1 Bianchini, C
A1 Bird, LM
A1 Buchert, R
A1 Carre, W
A1 Ceulemans, S
A1 Charles, P
A1 Cox, H
A1 Culliton, L
A1 Currò, A
A1 Deciphering Developmental Disorders (DDD) Study
A1 Demurger, F
A1 Dowling, JJ
A1 Duban-Bedu, B
A1 Dubourg, C
A1 Eiset, SE
A1 Escobar, LF
A1 Ferrarini, A
A1 Haack, TB
A1 Hashim, M
A1 Heide, S
A1 Helbig, KL
A1 Helbig, I
A1 Heredia, R
A1 Héron, D
A1 Isidor, B
A1 Jonasson, AR
A1 Joset, P
A1 Keren, B
A1 Kok, F
A1 Kroes, HY
A1 Lavillaureix, A
A1 Lu, X
A1 Maas, SM
A1 Maegawa, GHB
A1 Marcelis, CLM
A1 Mark, PR
A1 Masruha, MR
A1 McLaughlin, HM
A1 McWalter, K
A1 Melchinger, EU
A1 Mercimek-Andrews, S
A1 Nava, C
A1 Pendziwiat, M
A1 Person, R
A1 Ramelli, GP
A1 Ramos, LLP
A1 Rauch, A
A1 Reavey, C
A1 Renieri, A
A1 Rieß, A
A1 Sanchez-Valle, A
A1 Sattar, S
A1 Saunders, C
A1 Schwarz, N
A1 Smol, T
A1 Srour, M
A1 Steindl, K
A1 Syrbe, S
A1 Taylor, JC
A1 Telegrafi, A
A1 Thiffault, I
A1 Trauner, DA
A1 van der Linden, H
A1 van Koningsbruggen, S
A1 Villard, L
A1 Vogel, I
A1 Vogt, J
A1 Weber, YG
A1 Wentzensen, IM
A1 Widjaja, E
A1 Zak, J
A1 Baxter, S
A1 Banka, S
A1 Rodan, LH
PB Elsevier
YR 2019
JF https://openaccess.sgul.ac.uk/id/eprint/113838/1/O%27Donnell-LuriaetalAAM2019.pdf
LK http://dx.doi.org/https://openaccess.sgul.ac.uk/id/eprint/113838/
DO https://openaccess.sgul.ac.uk/id/eprint/113838/
SF ELIB - SuUB Bremen

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