Z. Yuksel Et Al. , "Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8, pp.1603-1608, 2019
Yuksel, Z. Et Al. 2019. Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8 , 1603-1608.
Yuksel, Z., Yazol, M., & Gumus, E., (2019). Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8, 1603-1608.
Yuksel, Zafer, MERVE YAZOL, And Evren Gumus. "Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8, 1603-1608, 2019
Yuksel, Zafer Et Al. "Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8, pp.1603-1608, 2019
Yuksel, Z. Yazol, M. And Gumus, E. (2019) . "Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.179, no.8, pp.1603-1608.
@article{article, author={Zafer Yuksel Et Al. }, title={Pathogenic homozygous variations in ACTL6B cause DECAM syndrome: Developmental delay, Epileptic encephalopathy, Cerebral Atrophy, and abnormal Myelination}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2019, pages={1603-1608} }