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1 Ergebnisse
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Case report: Novel compound heterozygous missense mutations..:
Xu, Xin
;
Lu, Fen
;
Du, Senjie
...
Frontiers in Pediatrics. 10 (2022) - p. , 2022
Link:
https://doi.org/10.3389/fped.2022.997274
RT Journal T1
Case report: Novel compound heterozygous missense mutations in the DDHD2 gene in a Chinese patient associated with spastic paraplegia type 54
UL https://suche.suub.uni-bremen.de/peid=cr-10.3389_fped.2022.997274&Exemplar=1&LAN=DE A1 Xu, Xin A1 Lu, Fen A1 Du, Senjie A1 Zhao, Xiaoke A1 Li, Hongying A1 Zhang, Li A1 Tang, Jian PB Frontiers Media SA YR 2022 SN 2296-2360 JF Frontiers in Pediatrics VO 10 LK http://dx.doi.org/https://doi.org/10.3389/fped.2022.997274 DO https://doi.org/10.3389/fped.2022.997274 SF ELIB - SuUB Bremen
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