Göktaş, S. Et Al. Severe Congenital Neutropenia due to HAX-1Mutations. 2020. In Rare Diseases in Children Focusing on Pediatric Immunology Neurology , Nobel Tıpe Kitabevi, Ankara, 132-146.

Göktaş, S., EKEN, A., & Patıroğlu, T., (2020). Severe Congenital Neutropenia due to HAX-1Mutations. Rare Diseases in Children Focusing on Pediatric Immunology Neurology (pp.132-146), Ankara: Nobel Tıpe Kitabevi.

Göktaş, Serdar, AHMET EKEN, And Türkan Patıroğlu. "Severe Congenital Neutropenia due to HAX-1Mutations." In Rare Diseases in Children Focusing on Pediatric Immunology Neurology , 132-146. Ankara: Nobel Tıpe Kitabevi, 2020

Göktaş, Serdar Et Al. "Severe Congenital Neutropenia due to HAX-1Mutations." Rare Diseases in Children Focusing on Pediatric Immunology Neurology , Nobel Tıpe Kitabevi, 2020, pp.132-146.

Göktaş, S. EKEN, A. And Patıroğlu, T. (2020) "Severe Congenital Neutropenia due to HAX-1Mutations", Rare Diseases in Children Focusing on Pediatric Immunology Neurology . Ankara: Nobel Tıpe Kitabevi.

@bookchapter{bookchapter, author ={Serdar Göktaş Et Al. }, chaptertitle={Severe Congenital Neutropenia due to HAX-1Mutations}, booktitle={ Rare Diseases in Children Focusing on Pediatric Immunology Neurology}, publisher={Nobel Tıpe Kitabevi}, city={Ankara},year={2020} }