Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Liburd, Nikki A."'
Autor:
Spyres, Lea, Gaddis, Sally, Bedford, Ella, Arantes, Stacey, Liburd, Nikki, Powell, K. Leslie, Thames, Howard, Mitchell, David, Walborg, Earl, Rouabhia, Mahmoud, Aldaz, C. Marcelo, MacLeod, Michael C.
Publikováno v:
In Analytical Biochemistry 2005 345(2):284-295
Autor:
Wilcox, Edward R *, Burton, Quianna L, Naz, Sadaf, Riazuddin, Saima, Smith, Tenesha N, Ploplis, Barbara, Belyantseva, Inna, Ben-Yosef, Tamar, Liburd, Nikki A, Morell, Robert J, Kachar, Bechara, Wu, Doris K, Griffith, Andrew J, Riazuddin, Sheikh, Friedman, Thomas B
Publikováno v:
In Cell 2001 104(1):165-172
Autor:
Liburd, Nikki, Ghosh, Manju, Riazuddin, Saima, Naz, Sadaf, Khan, Shaheen, Ahmed, Zubair, Riazuddin, Sheikh, Liang, Yong, Menon, Puthezhath, Smith, Tenesha, Smith, Ann, Chen, Ken-Shiung, Lupski, James, Wilcox, Edward, Potocki, Lorraine, Friedman, Thomas
Mutations in myosin XVA are responsible for the shaker 2 (sh2) phenotype in mice and nonsyndromic autosomal recessive profound hearing loss DFNB3 on chromosome 17p11.2. We have ascertained seven families with profound congenital hearing loss from Pak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::c4fb795e7cdf136df9762a31d8033e7a
https://zenodo.org/record/1232735
https://zenodo.org/record/1232735
Autor:
Riazuddin, Saima, Castelein, Caley M., Ahmed, Zubair M., Lalwani, Anil K., Mastroianni, Mary A., Naz, Sadaf, Smith, Tenesha N., Liburd, Nikki A., Friedman, Thomas B., Griffith, Andrew J., Riazuddin, Sheikh, Wilcox, Edward R.
Publikováno v:
Nature Genetics; Dec2000, Vol. 26 Issue 4, p431, 4p