Single Nucleotide Polymorphism (SNP)
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-55065-7_2049
Reference13 articles.
1. Al-Haggar, M., Madej-Pilarczyk, A., Kozlowski, L., Bujnicki, J. M., Yahia, S., Abdel-Hadi, D., Shams, A., Ahmad, N., Hamed, S., & Puzianowska-Kuznicka, M. (2012). A homozygous p.Arg527Leu LMNA mutation in the two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome. European Journal of Human Genetics, 20, 1134–1140.
2. Cao, R., Shi, Y., Chen, S., Ma, Y., Chen, J., Yang, J., Chen, G., & Shi, T. (2016). dbSAP: Single amino-acid polymorphism database for protein variation detection. Nucleic Acids Research, 45, 827–832.
3. Cordovado, S. K., Hendrix, M., Greene, C. N., Mochal, S., Earley, M. C., Farrell, P. M., Kharrazi, M., Hannon, W. H., & Mueller, P. W. (2012). CFTR mutation analysis and haplotype associations in CF patients. Molecular Genetics and Metabolism, 105, 249–254.
4. Giegling, I., Hartmann, A. M., Möller, H. J., & Rujescu, D. (2006). Anger- and aggression-related traits are associated with polymorphisms in the 5-HT-2A gene. Journal of Affective Disorders, 96, 75–81.
5. Glusman, G., Caballero, J., Mauldin, D. E., Hood, L., & Roach, J. C. (2011). Kaviar: An accessible system for testing SNV novelty. Bioinformatics, 27, 3216–3217.
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