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Active since
2008
Çağlayan Sh is an author specializing in mutation, genetic epilepsies, and molecular neurogenetics.
Publications per year
2008–2008
A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC).
Çağlayan Sh, Sema Saltık, Özlem Çokar et al. · PubMed · 2008 · 16 citations
Life Sciences, Genetics, Molecular Genetics +17
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