المؤلفون: Scala M., Mojarrad M., Riazuddin S., Brigatti K. W., Ammous Z., Cohen J. S., Hosny H., Usmani M. A., Shahzad M., Stanley V., Eslahi A., Person R. E., Elbendary H. M., Comi A. M., Poskitt L., Vincenzo Salpietro, Genomics Q. S., Rosenfeld J. A., Williams K. B., Marafi D., Xia F., Waberski M. B., Zaki M. S., Gleeson J., Puffenberger E., Houlden H., Maroofian R.

المساهمون: Scala, M., Mojarrad, M., Riazuddin, S., Brigatti, K. W., Ammous, Z., Cohen, J. S., Hosny, H., Usmani, M. A., Shahzad, M., Stanley, V., Eslahi, A., Person, R. E., Elbendary, H. M., Comi, A. M., Poskitt, L., SALPIETRO DAMIANO, Vincenzo, Genomics, Q. S., Rosenfeld, J. A., Williams, K. B., Marafi, D., Xia, F., Waberski, M. B., Zaki, M. S., Gleeson, J., Puffenberger, E., Houlden, H., Maroofian, R.

مصطلحات موضوعية: Adolescent, Child, Preschool, Female, Genes, Recessive, Human, Intellectual Disability, Loss of Function Mutation, Male, Nuclear Proteins

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/32227164; info:eu-repo/semantics/altIdentifier/wos/WOS:000541770600007; volume:143; firstpage:e31; lastpage:e31; journal:BRAIN; http://hdl.handle.net/11567/1027121; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85088885094

الاتاحة: http://hdl.handle.net/11567/1027121
https://doi.org/10.1093/brain/awaa070