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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 …

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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 …

01 Ocak 2019 Makale Google Scholar
Authors
PROFESÖR MERYEM ALBAYRAK

Atıf kopyala

P. M. ALBAYRAK (2019). 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 …. *Pediatric blood & cancer 66 (10), e27923, 2019*.

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Dergi Pediatric blood & cancer 66 (10), e27923, 2019
Veri tabanı Google Scholar
Kaynak GoogleScholar
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Atıf verisi 14 Kasım 2026 tarihinde güncellendi.

D Yılmaz Karapınar, T Patıroğlu, A Metin, Ü Çalışkan, T Celkan, B Yılmaz, ... | Pediatric blood & cancer 66 (10), e27923, 2019

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