Faruk Incecik
1PUBLICATIONS
6CO-AUTHORS

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Publications (1)
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|Sep 17, 2019
A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia.Rabia Miray Kisla Ekinci, Sibel Balcı, Atil Bisgin
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