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Expanding the phenotypic spectrum associated with OPHN1 mut..:
Moortgat, Stéphanie
;
Lederer, Damien
;
Deprez, Marie
...
European Journal of Medical Genetics. 61 (2018) 8 - p. 442-450 , 2018
Link:
https://doi.org/10.1016/j.ejmg.2018.03.002
RT Journal T1 <Title>Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2018.03.002&Exemplar=1&LAN=DE A1 Moortgat, Stéphanie A1 Lederer, Damien A1 Deprez, Marie A1 Buzatu, Marga A1 Clapuyt, Philippe A1 Boulanger, Sébastien A1 Benoit, Valérie A1 Mary, Sandrine A1 Guichet, Agnès A1 Ziegler, Alban A1 Colin, Estelle A1 Bonneau, Dominique A1 Maystadt, Isabelle PB Elsevier BV YR 2018 SN 1769-7212 JF European Journal of Medical Genetics VO 61 IS 8 SP 442 OP 450 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2018.03.002 DO https://doi.org/10.1016/j.ejmg.2018.03.002 SF ELIB - SuUB Bremen
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