Journal
Molecular Genetics and Metabolism Reports
Publication Date
12-1-2024
Volume
41
First Page
101145
Document Type
Open Access Publication
DOI
10.1016/j.ymgmr.2024.101145
Rights and Permissions
Ezell KM, Furuta Y, Oglesbee D, Pivnick EK, Rinker D, Sheehan JH, Tinker RJ, Hamid R, Cogan JD, Rives L, Neumann S, Corner B, Koziura M, Phillips JA 3rd; Undiagnosed Diseases Network. Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive condition. Mol Genet Metab Rep. 2024 Oct 5;41:101145. doi: 10.1016/j.ymgmr.2024.101145. © 2024 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/bync/4.0/).
Recommended Citation
Ezell, Kimberly M; Furuta, Yutaka; Oglesbee, Devin; Pivnick, Eniko K; Rinker, David; Sheehan, Jonathan H; Tinker, Rory J; Hamid, Rizwan; Cogan, Joy D; Rives, Lynette; Neumann, Serena; Corner, Brian; Koziura, Mary; Phillips, John A 3rd; and Undiagnosed Diseases Network, "Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal recessive condition." Molecular Genetics and Metabolism Reports. 41, 101145 (2024).
https://digitalcommons.wustl.edu/oa_4/5782
