Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry
Journal article published in 2019 by
Deniz Yılmaz Karapınar 
,
Türkan Patıroğlu,
Ayşe Metin,
Ümran Çalışkan,
Tiraje Celkan,
Barış Yılmaz ,
Zeynep Karakaş,
Tuba H. Karapınar ,
Burcu Akıncı,
Ferda Özkınay,
Hüseyin Onay,
Mehmet Akif Yeşilipek,
Himmet Haluk Akar,
Gülen Tüysüz,
Hüseyin Tokgöz
and other authors.
,
Türkan Patıroğlu,
Ayşe Metin,
Ümran Çalışkan,
Tiraje Celkan,
Barış Yılmaz ,
Zeynep Karakaş,
Tuba H. Karapınar ,
Burcu Akıncı,
Ferda Özkınay,
Hüseyin Onay,
Mehmet Akif Yeşilipek,
Himmet Haluk Akar,
Gülen Tüysüz,
Hüseyin Tokgöz
and other authors.
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