Süsgün, S. Et Al. 2020. Biallelic NALCN variant detected by homozygosity mapping and whole exome sequencing in a consanguineous family from Turkey. European Society of Human Genetics Annual Meeting 2020 , (Berlin, Germany), 1.

Süsgün, S., Yücesan, E., Çalık, M., Özbek, U., & Uğur İşeri, S. A., (2020). Biallelic NALCN variant detected by homozygosity mapping and whole exome sequencing in a consanguineous family from Turkey . European Society of Human Genetics Annual Meeting 2020 (pp.1). Berlin, Germany

Süsgün, Seda Et Al. "Biallelic NALCN variant detected by homozygosity mapping and whole exome sequencing in a consanguineous family from Turkey," European Society of Human Genetics Annual Meeting 2020, Berlin, Germany, 2020

Süsgün, Seda Et Al. "Biallelic NALCN variant detected by homozygosity mapping and whole exome sequencing in a consanguineous family from Turkey." European Society of Human Genetics Annual Meeting 2020 , Berlin, Germany, pp.1, 2020

Süsgün, S. Et Al. (2020) . "Biallelic NALCN variant detected by homozygosity mapping and whole exome sequencing in a consanguineous family from Turkey." European Society of Human Genetics Annual Meeting 2020 , Berlin, Germany, p.1.

@conferencepaper{conferencepaper, author={Seda Süsgün Et Al. }, title={Biallelic NALCN variant detected by homozygosity mapping and whole exome sequencing in a consanguineous family from Turkey}, congress name={European Society of Human Genetics Annual Meeting 2020}, city={Berlin}, country={Germany}, year={2020}, pages={1} }