KÖSE, E. Et Al. 2016. Novel Mutation causing Biotinidase Deficiency in a Patient Identified by Newborn Screening. 13th Middle East Metabolic Group Meeting .

KÖSE, E., ONAY, H., & ARSLAN, N., (2016). Novel Mutation causing Biotinidase Deficiency in a Patient Identified by Newborn Screening . 13th Middle East Metabolic Group Meeting

KÖSE, ENGİN, HÜSEYİN ONAY, And NUR ARSLAN. "Novel Mutation causing Biotinidase Deficiency in a Patient Identified by Newborn Screening," 13th Middle East Metabolic Group Meeting, 2016

KÖSE, ENGİN Et Al. "Novel Mutation causing Biotinidase Deficiency in a Patient Identified by Newborn Screening." 13th Middle East Metabolic Group Meeting , 2016

KÖSE, E. ONAY, H. And ARSLAN, N. (2016) . "Novel Mutation causing Biotinidase Deficiency in a Patient Identified by Newborn Screening." 13th Middle East Metabolic Group Meeting .

@conferencepaper{conferencepaper, author={ENGİN KÖSE Et Al. }, title={Novel Mutation causing Biotinidase Deficiency in a Patient Identified by Newborn Screening}, congress name={13th Middle East Metabolic Group Meeting}, city={}, country={}, year={2016}}