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1 Ergebnisse
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Table_1_Novel Missense CNTNAP2 Variant Identified in Two Co..:
Noor Badshah
;
Kari A. Mattison
;
Sohail Ahmad
...
doi:10.3389/fneur.2022.918022.s001. , 2022
Link:
https://doi.org/10.3389/fneur.2022.918022.s001
RT Journal T1
Table_1_Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior.DOCX
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_20305038&Exemplar=1&LAN=DE A1 Noor Badshah A1 Kari A. Mattison A1 Sohail Ahmad A1 Pankaj Chopra A1 H. Richard Johnston A1 Shakoor Ahmad A1 Sher Hayat Khan A1 Muhammad Tahir Sarwar A1 David J. Cutler A1 Micheal Taylor A1 Gayatri Vadlamani A1 Michael E. Zwick A1 Andrew Escayg YR 2022 K1 Neurology and Neuromuscular Diseases K1 Neurogenetics K1 epilepsy genetics K1 CNTNAP2 K1 Afridi tribe K1 Pakistan K1 autosomal recessive JF doi:10.3389/fneur.2022.918022.s001 LK http://dx.doi.org/https://doi.org/10.3389/fneur.2022.918022.s001 DO https://doi.org/10.3389/fneur.2022.918022.s001 SF ELIB - SuUB Bremen
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