Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity

за авторством Boy, Nikolas, Heringer, Jana, Brackmann, Renate
Опубліковано в: Orphanet Journal of Rare Diseases (2017)

Шифр: Zs Open Access

Homozygous frame shift variant in ATP7B exon 1 leads to bypass of nonsense-mediated mRNA decay and to a protein capable of copper export

за авторством Stalke, Amelie, Pfister, Eva-Doreen, Brackmann, Renate
Опубліковано в: European Journal of Human Genetics (2019)

Шифр: Zs Open Access