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1 Ergebnisse
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Ataxia in Patients With Bi-Allelic NFASC Mutations and Abse..:
Kvarnung, Malin
;
Shahsavani, Mansoureh
;
Taylan, Fulya
...
Frontiers in Genetics, 2019, 10,. , 2019
Link:
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-395798
RT Journal T1
Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
UL https://suche.suub.uni-bremen.de/peid=base-ftuppsalauniv:oai:DiVA.org:uu-395798&Exemplar=1&LAN=DE A1 Kvarnung, Malin A1 Shahsavani, Mansoureh A1 Taylan, Fulya A1 Moslem, Mohsen A1 Breeuwsma, Nicole A1 Laan, Loora A1 Schuster, Jens A1 Jin, Zhe A1 Nilsson, Daniel A1 Lieden, Agne A1 Anderlid, Britt-Marie A1 Nordenskjold, Magnus A1 Lundberg, Elisabeth Syk A1 Birnir, Bryndis A1 Dahl, Niklas A1 Nordgren, Ann A1 Lindstrand, Anna A1 Falk, Anna PB Uppsala universitet, Medicinsk genetik och genomik; Uppsala universitet, Science for Life Laboratory, SciLifeLab; Uppsala universitet, Birnir: Molekylär fysiologi och neurovetenskap; Karolinska Univ Hosp, Dept Clin Genet, Stockholm, Sweden;Karolinska Inst, Ctr Mol Med, Dept Mol Med & Surg, Stockholm, Sweden; Karolinska Inst, Ctr Mol Med, Dept Mol Med & Surg, Stockholm, Sweden;Karolinska Inst, Biomed, Dept Neurosci, Stockholm, Sweden; Karolinska Inst, Ctr Mol Med, Dept Mol Med & Surg, Stockholm, Sweden; Karolinska Inst, Biomed, Dept Neurosci, Stockholm, Sweden YR 2019 K1 neurofascin K1 neuronal isoform NF186 K1 ataxia K1 patient-specific induced pluripotent stem cells K1 neuroepithelial stem cells K1 neurites K1 Neurosciences K1 Neurovetenskaper JF Frontiers in Genetics, 2019, 10, LK http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-395798 DO http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-395798 SF ELIB - SuUB Bremen
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