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Faruk Incecik

1PUBLICATIONS

6CO-AUTHORS

Haematological tumours

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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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Frequent Collaborators

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Rabia Miray Kisla Ekinci

1 joint publications

Sibel Balcı

1 joint publications

Atil Bisgin

1 joint publications

Ilgen Sasmaz

1 joint publications

Goksel Leblebisatan

1 joint publications

Mustafa Yilmaz

Frequent Collaborators

1 joint publications

Rabia Miray Kisla Ekinci

1 joint publications

Sibel Balcı

1 joint publications

Atil Bisgin

1 joint publications

Ilgen Sasmaz

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