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Autosomal dominant cutis laxa and critical stenosis of the left main coronary artery in a 21-year-old female with an intronic mutation in the elastin gene.
Am J Med Genet A. 2023 Apr;191(4):1059-1064. doi: 10.1002/ajmg.a.63095. Epub 2022 Dec 21.
Am J Med Genet A. 2023.
PMID: 36541930
Sporadic late onset nemaline myopathy with concurrent dermatological symptoms responding to immunosuppressive treatment.
Nandy A, Tankisi H, Krøigård AB, Dalager MG, Hvidbjerg MS, Schrøder HD, Obál I.
Nandy A, et al. Among authors: hvidbjerg ms.
BMC Neurol. 2023 Jun 16;23(1):233. doi: 10.1186/s12883-023-03283-7.
BMC Neurol. 2023.
PMID: 37328820
Free PMC article.
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