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pro vyhledávání: '"Lidia Suchoń"'
Autor:
Aleksandra Jezela-Stanek, Lidia Suchoń, Agnieszka Sobczyńska-Tomaszewska, Kamila Czerska, Katarzyna Kuśmierska, Joanna Taybert, Mariusz Ołtarzewski, Jolanta Sykut-Cegielska
Publikováno v:
Genes; Volume 13; Issue 5; Pages: 802
Biotinidase deficiency (BD) is a rare autosomal recessive metabolic disease. Previously the disease was identified only by clinical signs and symptoms, and since recently, it has been included in newborn screening programs (NBS) worldwide, though not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e97e69c34afdc90ab9358d13b9e0d58f
