Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless.

Autor: Wallis, Mathew^1,2,3 (AUTHOR), Bodek, Simon D.^1,4 (AUTHOR) simon.bodek@austin.org.au, Munro, Jacob^5,6 (AUTHOR), Rafehi, Haloom^5,6 (AUTHOR), Bennett, Mark F.^5,6,7 (AUTHOR), Ye, Zimeng⁷ (AUTHOR), Schneider, Amy⁷ (AUTHOR), Gardiner, Fiona⁷ (AUTHOR), Valente, Giulia¹ (AUTHOR), Murdoch, Emma¹ (AUTHOR), Uebergang, Eloise^1,8 (AUTHOR), Hunter, Jacquie¹ (AUTHOR), Stutterd, Chloe^1,8,9,10 (AUTHOR), Huq, Aamira^1,11 (AUTHOR), Salmon, Lucinda^1,12 (AUTHOR), Scheffer, Ingrid^1,7,13 (AUTHOR), Eratne, Dhamidhu^1,7,14 (AUTHOR), Meyn, Stephen¹⁵ (AUTHOR), Fong, Chun Y.¹ (AUTHOR), John, Tom^1,4,16 (AUTHOR)

Publikováno v: Orphanet Journal of Rare Diseases. 8/2/2024, Vol. 19 Issue 1, p1-14. 14p.