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Novel LMNA Gene Mutation in a Patient With Atypical Werner's Syndrome
Yun Jeong Doh, Hee Kyoung Kim, Eui Dal Jung, Seung Hee Choi, Jung Guk Kim, Bo Wan Kim, In Kyu Lee
Korean J Intern Med. 2009;24(1):68-72.   Published online 2009 March 6    DOI: https://doi.org/10.3904/kjim.2009.24.1.68

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Novel LMNA Gene Mutation in a Patient With Atypical Werner's Syndrome
The Korean journal of internal medicine. 2009;24(1):68   Crossref logo
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Cerebral Haemorrhage in a Young Patient With Atypical Werner Syndrome Due to Mutations in LMNA
Frontiers in Endocrinology. 2018;9:   Crossref logo
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PC045: Novel mutation of the cathepsin C gene identified in a Portuguese patient with atypical Papillon-Lefèvre syndrome
Journal of Clinical Periodontology. 2018;45:379-379   Crossref logo
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Regulation of Interferon-stimulated Gene (<italic>ISG</italic>)<italic>12</italic>, <italic>ISG15</italic>, and <italic>MX1</italic> and <italic>MX2</italic> by Conceptus Interferons (IFNTs) in Bovine Uterine Epithelial Cells
Asian-Australasian Journal of Animal Sciences. 2013;26(6):795-803   Crossref logo
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Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance
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Cardiac <sup>123</sup>I-metaiodobenzylguanidine Scintigraphy in a Patient with Familial Parkinsonism with <italic>Parkin</italic> Gene Mutation
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A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A
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A novel mutation of ETV6 gene in patient of atypical chronic myeloid leukemia: A case report
Clinica Chimica Acta. 2019;493:S232-S233   Crossref logo
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A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndrome
Human Mutation. 1996;7(2):181-182   Crossref logo
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