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Identification of a novel nonsense SLC16A2 gene mutation in..:
Peng, Wu
;
Shi, Shuxia
;
Yang, Liqi
.
Medicine. 103 (2024) 29 - p. e39047 , 2024
Link:
https://doi.org/10.1097/md.0000000000039047
RT Journal T1
Identification of a novel nonsense SLC16A2 gene mutation in an infant with severe neurologic phenotype: A case report
UL https://suche.suub.uni-bremen.de/peid=cr-10.1097_md.0000000000039047&Exemplar=1&LAN=DE A1 Peng, Wu A1 Shi, Shuxia A1 Yang, Liqi A1 Liu, Deyun PB Ovid Technologies (Wolters Kluwer Health) YR 2024 SN 0025-7974 SN 1536-5964 JF Medicine VO 103 IS 29 SP e39047 LK http://dx.doi.org/https://doi.org/10.1097/md.0000000000039047 DO https://doi.org/10.1097/md.0000000000039047 SF ELIB - SuUB Bremen
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