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1 Ergebnisse
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A novel de novo FEM1C variant is linked to neurodevelopment..:
Dubey, Abhishek Anil
;
Krygier, Magdalena
;
Szulc, Natalia A
...
Human Molecular Genetics. 32 (2022) 7 - p. 1152-1161 , 2022
Link:
https://doi.org/10.1093/hmg/ddac276
RT Journal T1
A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddac276&Exemplar=1&LAN=DE A1 Dubey, Abhishek Anil A1 Krygier, Magdalena A1 Szulc, Natalia A A1 Rutkowska, Karolina A1 Kosińska, Joanna A1 Pollak, Agnieszka A1 Rydzanicz, Małgorzata A1 Kmieć, Tomasz A1 Mazurkiewicz-Bełdzińska, Maria A1 Pokrzywa, Wojciech A1 Płoski, Rafał PB Oxford University Press (OUP) YR 2022 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics VO 32 IS 7 SP 1152 OP 1161 LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddac276 DO https://doi.org/10.1093/hmg/ddac276 SF ELIB - SuUB Bremen
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