KIŞLA EKİNCİ, R. M. Et Al. 2020. Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey. RHEUMATOLOGY , vol.59, no.1 , 254-256.

KIŞLA EKİNCİ, R. M., Balci, S., Hershfield, M., BİŞGİN, A., DOĞRUEL, D., ALTINTAŞ, D. U., ... YILMAZ, M.(2020). Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey. RHEUMATOLOGY , vol.59, no.1, 254-256.

KIŞLA EKİNCİ, RABİA Et Al. "Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey," RHEUMATOLOGY , vol.59, no.1, 254-256, 2020

KIŞLA EKİNCİ, RABİA M. Et Al. "Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey." RHEUMATOLOGY , vol.59, no.1, pp.254-256, 2020

KIŞLA EKİNCİ, R. M. Et Al. (2020) . "Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey." RHEUMATOLOGY , vol.59, no.1, pp.254-256.

@article{article, author={RABİA MİRAY KIŞLA EKİNCİ Et Al. }, title={Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey}, journal={RHEUMATOLOGY}, year=2020, pages={254-256} }