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A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency Autoría: Deniz Özalp Kızılay, Deniz Yılmaz Karapınar, Nihal Karadaş, Murat Karaoğlan, Sinan Akbayram, Damla Gökşen, Ayşe Gadashova, Serpil Albayrak, Esra Pekpak Şahinoğlu, Zerrin Orbak, Zafer Bıçakçı, Leyla Akın, Canan Albayrak, Cansu Koç, Ayşegül Ünüvar, Ahmet Anık, Yusuf Ziya Aral, Emine Ayça Cimbek, Ayşenur Bahadır, Cem Mete, Samim Özen