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
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| Description | scientific article published on 19 July 2019 |
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author: Nihal Özdemir Deniz Yılmaz Karapınar Ayca Kiykim Baris Yilmaz Nihal Özdemir Karadaş Tuba H Karapınar Vedat Uygun Talia İleri Serap Karaman Tiraje Celkan |
| Publication date | July 19, 2019 |
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