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المؤلفون: Eric D. Spear, H. J. Worman, Yuefan Wang, W. Hsu, W. Wu, C.-S. Lin, Susan Michaelis, K. Shiladardi, T. Maruyama, C. B. Damoci, T. Hsu, J.-Y. Shin, Kamsi O. Odinammadu
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Longevity, Biology, Mice, Progeria, Internal medicine, medicine, Animals, Loss function, Prenylation, Binding Sites, Multidisciplinary, integumentary system, Farnesyltransferase inhibitor, Membrane Proteins, Metalloendopeptidases, nutritional and metabolic diseases, Lamin Type A, Progerin, medicine.disease, Phenotype, Embryonic stem cell, Endocrinology, Mutation, Nuclear lamina, Lamin
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5507af2eaa98cfe2d228d7ebda23e7b7
https://doi.org/10.1101/2021.11.11.465186