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1دورية أكاديميةA novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations
المؤلفون: Munot, P., Saunders, D. E., Milewicz, D. M., Regalado, E. S., Ostergaard, J. R., Braun, K. P., Kerr, T., Lichtenbelt, K. D., Philip, S., Rittey, C., Jacques, T. S., Cox, T. C., Ganesan, V.
المصدر: Brain ; volume 135, issue 8, page 2506-2514 ; ISSN 0006-8950 1460-2156
الإتاحة: https://doi.org/10.1093/brain/aws172Test
http://academic.oup.com/brain/article-pdf/135/8/2506/870093/aws172.pdfTest -
2دورية أكاديمية
المؤلفون: Colombo R.
المساهمون: Wallace, S. E., Regalado, E. S., Gong, L., Janda, A. L., Guo, D. -C., Russo, C. F., Kulmacz, R. J., Hanna, N., Jondeau, G., Boileau, C., Arnaud, P., Lee, K., Leal, S. M., Hannuksela, M., Carlberg, B., Johnston, T., Antolik, C., Hostetler, E. M., Colombo, Roberto, Milewicz, D. M.
مصطلحات موضوعية: acute aortic dissection, hereditary thoracic aortic disease, MYLK, myosin light-chain kinase, thoracic aortic surgery, Adult, Aged, Aneurysm, Dissecting, Aorta, Aortic Diseases, Calcium-Binding Proteins, Female, Heterozygote, Humans, Male, Middle Aged, Myosin-Light-Chain Kinase, Pedigree, Pregnancy, Genetic Testing, High-Throughput Nucleotide Sequencing, Settore BIO/10 - BIOCHIMICA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29925964; info:eu-repo/semantics/altIdentifier/wos/WOS:000455403400020; volume:21; issue:1; firstpage:144; lastpage:151; numberofpages:8; issueyear:2019; journal:GENETICS IN MEDICINE; http://hdl.handle.net/10807/170888Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85048728966
