المؤلفون: Anastasia V. Tumakova, Ilya V. Bizin, Maria A. Makhova, Lidiya V. Lyazina, Marina N Guseva, Evgeny N. Suspitsin, Mikhail Kostik, Irina Kondratenko, Olga P. Kozlova, Tatiana V. Gabrusskaya, Svetlana S. Vahliarskaya, Anastasia S. Levina, M. Dubko, Olga V. Goleva, Liliya V. Ditkovskaya, Evgeny N. Imyanitov, Nataliya V. Skripchenko, Anna P. Sokolenko, Natalia E. Sokolova

المصدر: Clinical geneticsREFERENCES. 98(3)

مصطلحات موضوعية: 0301 basic medicine, Male, DCLRE1C, Adolescent, Primary Immunodeficiency Diseases, Disease, Semaphorins, 030105 genetics & heredity, Russia, 03 medical and health sciences, CHARGE syndrome, Immune system, Agammaglobulinemia, Genetics, medicine, Humans, Netherton syndrome, Genetic Predisposition to Disease, Child, Genetics (clinical), Immunodeficiency, business.industry, Autoimmune Cytopenia, High-Throughput Nucleotide Sequencing, Infant, Genetic Diseases, X-Linked, medicine.disease, Endonucleases, DNA-Binding Proteins, 030104 developmental biology, Child, Preschool, Immunology, Primary immunodeficiency, Female, Severe Combined Immunodeficiency, CHARGE Syndrome, business, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5285a98b332619f8d4355dd1448c9bba
https://pubmed.ncbi.nlm.nih.gov/32441320