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A Novel De Novo NFKBIA Missense Mutation Associated to Ecto..:
Chai Teng Chear
;
Bader Abdul Kader El Farran
;
Marina Sham
...
Human Genomics and Genetic Diseases. , 2022
Link:
https://doi.org/10.3390/genes13101900
RT Journal T1
A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia
UL https://suche.suub.uni-bremen.de/peid=base-ftmdpi:oai:mdpi.com:_2073-4425_13_10_1900_&Exemplar=1&LAN=DE A1 Chai Teng Chear A1 Bader Abdul Kader El Farran A1 Marina Sham A1 Kavetha Ramalingam A1 Lokman Mohd Noh A1 Intan Hakimah Ismail A1 Mei Yee Chiow A1 Mohd Farid Baharin A1 Adiratna Mat Ripen A1 Saharuddin Bin Mohamad PB Multidisciplinary Digital Publishing Institute YR 2022 K1 hyper IgM-like phenotype K1 NFKBIA K1 IκBα K1 NF-κB K1 post-translational modification JF Human Genomics and Genetic Diseases LK http://dx.doi.org/https://doi.org/10.3390/genes13101900 DO https://doi.org/10.3390/genes13101900 SF ELIB - SuUB Bremen
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