Hasil Pencarian - Natalia Dolzhanskaya
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Tissue and developmental regulation of fragile X mental retardation 1 exon 12 and 15 isoforms oleh Wen Xie, Natalia Dolzhanskaya, Giuseppe LaFauci, Carl Dobkin, Robert B. Denman
Diterbitkan 2009-07-01Dapatkan teks lengkap
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2
Increased Expression of the Large Conductance, Calcium-Activated K+ (BK) Channel in Adult-Onset Neuronal Ceroid Lipofuscinosis. oleh Julien Donnelier, Samuel T Braun, Natalia Dolzhanskaya, Eva Ahrendt, Andrew P Braun, Milen Velinov, Janice E A Braun
Diterbitkan 2015-01-01Dapatkan teks lengkap
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3
Correction: Mutations in the Gene Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families. oleh Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric Powell, Ioanna Konidari, William Hulme, John F. Staropoli, Winnie Xin, Guang Y. Wen, Rosemary Barone, Scott H. Coppel, Katherine Sims, W. Ted Brown, Stephan Züchner
Diterbitkan 2012-01-01Dapatkan teks lengkap
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4
Mutations in the gene DNAJC5 cause autosomal dominant Kufs disease in a proportion of cases: study of the Parry family and 8 other families. oleh Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric Powell, Ioanna Konidari, William Hulme, John F Staropoli, Winnie Xin, Guang Y Wen, Rosemary Barone, Scott H Coppel, Katherine Sims, W Ted Brown, Stephan Züchner
Diterbitkan 2012-01-01Dapatkan teks lengkap
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