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1 Ergebnisse
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ZMYND11variants are a novel cause of centrotemporal and gen..:
Oates, Stephanie
;
Absoud, Michael
;
Goyal, Sushma
...
Clinical Genetics. 100 (2021) 4 - p. 412-429 , 2021
Link:
https://doi.org/10.1111/cge.14023
RT Journal T1
ZMYND11variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14023&Exemplar=1&LAN=DE A1 Oates, Stephanie A1 Absoud, Michael A1 Goyal, Sushma A1 Bayley, Sophie A1 Baulcomb, Jennifer A1 Sims, Annemarie A1 Riddett, Amy A1 Allis, Katrina A1 Brasch‐Andersen, Charlotte A1 Balasubramanian, Meena A1 Bai, Renkui A1 Callewaert, Bert A1 Hüffmeier, Ulrike A1 Le Duc, Diana A1 Radtke, Maximilian A1 Korff, Christian A1 Kennedy, Joanna A1 Low, Karen A1 Møller, Rikke S. A1 Nielsen, Jens Erik Klint A1 Popp, Bernt A1 Quteineh, Lina A1 Rønde, Gitte A1 Schönewolf‐Greulich, Bitten A1 Shillington, Amelle A1 Taylor, Matthew RG A1 Todd, Emily A1 Torring, Pernille M. A1 Tümer, Zeynep A1 Vasileiou, Georgia PB Wiley YR 2021 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 100 IS 4 SP 412 OP 429 LK http://dx.doi.org/https://doi.org/10.1111/cge.14023 DO https://doi.org/10.1111/cge.14023 SF ELIB - SuUB Bremen
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