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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 Neutropenia Registry

Karapinar, Deniz Yilmaz; Patiroglu, Turkan; Metin, Ayse; Caliskan, Umran; Celkan, Tiraje; Yilmaz, Baris; Karakas, Zeynep; Karapinar, Tuba H.; Akinci, Burcu; Ozkinay, Ferda; Onay, Huseyin; Yesilipek, Mehmet Akif; Akar, Himmet Haluk; Tuysuz, Gulen; Tokgoz, Huseyin; Ozdemir, Gul Nihal; Kiykim, Ayca Aslan; Karaman, Serap; Kilinc, Yurdanur; Oymak, Yesim; Oymak, Yesim


BibTeX

@article{karapinar_deniz_yilmaz_2019_71535,
  author       = {Karapinar, Deniz Yilmaz and
                  Patiroglu, Turkan and
                  Metin, Ayse and
                  Caliskan, Umran and
                  Celkan, Tiraje and
                  Yilmaz, Baris and
                  Karakas, Zeynep and
                  Karapinar, Tuba H. and
                  Akinci, Burcu and
                  Ozkinay, Ferda and
                  Onay, Huseyin and
                  Yesilipek, Mehmet Akif and
                  Akar, Himmet Haluk and
                  Tuysuz, Gulen and
                  Tokgoz, Huseyin and
                  Ozdemir, Gul Nihal and
                  Kiykim, Ayca Aslan and
                  Karaman, Serap and
                  Kilinc, Yurdanur and
                  Oymak, Yesim and
                  Oymak, Yesim},
  title        = {{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      = {PEDIATRIC BLOOD \& CANCER},
  year         = 2019,
  volume       = 66,
  number       = 10,
  month        = jan,
}
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