H63D Syndrome: What we know about it in 2021

Autor:	Dr. Carolina Diamandis, Jacob S Adams, Riku Honda, Anastasios Papadopoulos, Lucas Smith, Marianne Kaufmann, Marius Lazar, Carolina Diamandis, David Seideman
Rok vydání:	2021
Předmět:	congenital hereditary and neonatal diseases and abnormalities nutritional and metabolic diseases
Popis:	H63D syndrome is a serious and clinically progressive disorder of iron metabolism caused by non-transferrin-bound iron (NTBI). In 2019, after scientists from around the world joined together to form the H63D Syndrome Research Consortium (a non-profit entity), a consensus paper “H63D Syndrome” was adopted at a meeting in Oslo in December 2019. With this new paper, we summarize what the leading experts in the field know about the syndrome in 2021.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f326660ae1adcbf477385a3d00612358 https://doi.org/10.22541/au.162191694.46218714/v1 Zobrazit plný text záznamu