Articles on yeni nesil sekans sistemi

1 articles published in Selcuk Medical Journal with the keyword "yeni nesil sekans sistemi": A case report of Neurofibromatosis type 1 diagnosed with a noval mutation detection in NF1 gene

A CASE REPORT OF NEUROFIBROMATOSIS TYPE 1 DIAGNOSED WITH A NOVAL MUTATION DETECTION IN NF1 GENE

NAFİZ YAŞA, BÜŞRA ESER ÇAVDARTEPE, FAHRETTİN DUYMUŞ, NADİR KOÇAK, TÜLİN ÇORA

2019, Vol 35, Issue 4, Page 274-277

Neurofibromatosis type I (NF1) is a complex disorder caused by mutations of the neurofibromin protein-encoding gene on the chromosome 17. NF1 is an autosomal dominant disorder. The prevalence of NF1 is approximately 1:2500 to 1:3500. Both genders are equally affected. Herein, we report a...

Related Keywords

NF1 Yeni mutasyon heterozigot mutasyon A novel mutation heterozygous mutation NGS system