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1 Ergebnisse
1
CCDC88A mutations cause PEHO-like syndrome in humans and mo..:
Nahorski, Michael S
;
Asai, Masato
;
Wakeling, Emma
...
https://www.repository.cam.ac.uk/handle/1810/253692. , 2016
Link:
https://www.repository.cam.ac.uk/handle/1810/253692
RT Journal T1
CCDC88A mutations cause PEHO-like syndrome in humans and mouse
UL https://suche.suub.uni-bremen.de/peid=base-ftunivcam:oai:www.repository.cam.ac.uk:1810_253692&Exemplar=1&LAN=DE A1 Nahorski, Michael S A1 Asai, Masato A1 Wakeling, Emma A1 Parker, Alasdair A1 Asai, Naoya A1 Canham, Natalie A1 Holder, Susan E A1 Chen, Ya-Chun A1 Dyer, Joshua A1 Brady, Angela F A1 Takahashi, Masahide A1 Woods, C Geoffrey PB Oxford University Press (OUP); http://dx.doi.org/10.1093/brain/aww014; Brain YR 2016 K1 PEHO syndrome K1 epilepsy K1 girdin K1 microcephaly K1 neurodevelopmental disorder K1 Animals K1 Brain K1 Brain Edema K1 Child K1 Female K1 Humans K1 Infant K1 Male K1 Mice K1 Knockout K1 Microfilament Proteins K1 Mutation K1 Neurodegenerative Diseases K1 Optic Atrophy K1 Pedigree K1 Spasms K1 Infantile K1 Vesicular Transport Proteins JF https://www.repository.cam.ac.uk/handle/1810/253692 LK http://dx.doi.org/https://www.repository.cam.ac.uk/handle/1810/253692 DO https://www.repository.cam.ac.uk/handle/1810/253692 SF ELIB - SuUB Bremen
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