Identification and characterization of BTD gene  mutations in Jordanian children with biotinidase deficiency

JOURNAL OF PERSONALIZED MEDICINE

AL-EITAN, L.N.; ALQA´QA´, K.; AMAYREH, W.; KHASAWNEH, R.; ALJAMAL, H.; AL-ABED, M.; HADDAD, Y.; RAWASHDEH, T.; JARADAT, Z.; HADDAD, H., 2020: Identification and characterization of BTD gene  mutations in Jordanian children with biotinidase deficiency. JOURNAL OF PERSONALIZED MEDICINE 10(1), p. 1 - 9, doi: 10.3390/jpm10010004; FULL TEXT

Research Groups:

• Smart Nanodevices - Vojtěch Adam

CEITEC authors:

• M.Sc. Yazan Abdulmajeed Eyadh Haddad, Ph.D.