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1 Ergebnisse
1
Novel Missense CNTNAP2 Variant Identified in Two Consanguin..:
Noor Badshah
;
Kari A. Mattison
;
Sohail Ahmad
...
https://www.frontiersin.org/articles/10.3389/fneur.2022.918022/full. , 2022
Link:
https://doi.org/10.3389/fneur.2022.918022
RT Journal T1 <Title>Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:6c2912c584884f93a5ec7445a02179a0&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 PB Frontiers Media S.A. YR 2022 K1 epilepsy genetics K1 CNTNAP2 K1 Afridi tribe K1 Pakistan K1 autosomal recessive K1 Neurology. Diseases of the nervous system K1 RC346-429 JF https://www.frontiersin.org/articles/10.3389/fneur.2022.918022/full LK http://dx.doi.org/https://doi.org/10.3389/fneur.2022.918022 DO https://doi.org/10.3389/fneur.2022.918022 SF ELIB - SuUB Bremen
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