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A biallelic loss-of-function variant in MYZAP is associated with a recessive form of severe dilated cardiomyopathy.
Maver A, Zigman T, Rangrez AY, Coric M, Homolak J, Saric D, Skific I, Udovicic M, Zekusic M, Saleem U, Laufer SD, Hansen A, Frey N, Baric I, Peterlin B. Maver A, et al. Among authors: zekusic m. Cold Spring Harb Mol Case Stud. 2022 Jul 15;8(5):a006221. doi: 10.1101/mcs.a006221. Online ahead of print. Cold Spring Harb Mol Case Stud. 2022. PMID: 35840178 Free PMC article.
Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene.
Žigman T, Petković Ramadža D, Lušić M, Zekušić M, Ninković D, Gardijan D, Potočki K, Omerza L, Beljan L, Žarković K, Kerkhof J, Ljubojević M, de Sain-van der Velden M, Vuković J, Fumić K, Sadiković B, Barić I. Žigman T, et al. Among authors: zekusic m. J Pediatr Endocrinol Metab. 2018 Oct 25;31(10):1155-1159. doi: 10.1515/jpem-2017-0397. J Pediatr Endocrinol Metab. 2018. PMID: 30243016
Early initiation of ambroxol treatment diminishes neurological manifestations of type 3 Gaucher disease: A long-term outcome of two siblings.
Ramadža DP, Zekušić M, Žigman T, Škaričić A, Bogdanić A, Mustać G, Bošnjak-Nađ K, Ozretić D, Ohno K, Fumić K, Barić I. Ramadža DP, et al. Among authors: zekusic m. Eur J Paediatr Neurol. 2021 May;32:66-72. doi: 10.1016/j.ejpn.2021.03.013. Epub 2021 Mar 31. Eur J Paediatr Neurol. 2021. PMID: 33836415
New characterization and safety evaluation of human limbal stem cells used in clinical application: fidelity of mitotic process and mitotic spindle morphologies.
Zekušić M, Bujić Mihica M, Skoko M, Vukušić K, Risteski P, Martinčić J, Tolić IM, Bendelja K, Ramić S, Dolenec T, Vrgoč Zimić I, Puljić D, Petric Vicković I, Iveković R, Batarilo I, Prosenc Zmrzljak U, Hoffmeister A, Vučemilo T. Zekušić M, et al. Stem Cell Res Ther. 2023 Dec 13;14(1):368. doi: 10.1186/s13287-023-03586-z. Stem Cell Res Ther. 2023. PMID: 38093301 Free PMC article.