1
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
द्वारा Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.
में प्रकाशित Acta Neuropathol (2019)
पूर्ण पाठ प्राप्त करें में प्रकाशित Acta Neuropathol (2019)
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2
द्वारा Escolar, D.M., Zimmerman, A., Bertorini, T., Clemens, P.R., Connolly, A.M., Mesa, L., Gorni, K., Kornberg, A., Kolski, H., Kuntz, N., Nevo, Y., Tesi-Rocha, C., Nagaraju, K., Rayavarapu, S., Hache, L.P., Mayhew, J.E., Florence, J., Hu, F., Arrieta, A., Henricson, E., Leshner, R.T., Mah, J.K., Igarashi, Masanori, Abdel-Hamid, Hoda, Pestronk, Alan, Dubroski, Alberto, Ryan, Monique, Kaminski, Sarah, Bartczak, Marisa, Parker, Katherine, Duong, Tina, Thannhauser, Jennifer, Goia, Edit, Chiu, Angela, Caton, Megan, Rashed, Hani, Feliciano, Casandra, Clifft, Judy, Coleman, Ann, Bise, Christopher, Paulukonis, Kara, Wulf, Charlie, Renna, Renee, Malkus, Betsy, Siener, Catherine, Corderi, Jose, Capone, Luca, Ferretti, Marco, Villano, Dani, Carroll, Kate, Kennedy, Rachel, Kennedy, Cam, Chen, Lucia, Peterson, Wendy Korn, Coleman-Wood, Krista, Kotakarvi, Brian, Yaffe, Debbie, Weisband, Elana
प्रकाशित 2012
पूर्ण पाठ प्राप्त करें प्रकाशित 2012
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Artigo
3
द्वारा Hodgkinson, V., Lounsberry, J., M’Dahoma, S., Russell, A., Jewett, G., Benstead, T., Brais, B., Campbell, C., Johnston, W., Lochmüller, H., McCormick, A., Nguyen, C. T., O’Ferrall, E., Oskoui, M., Abrahao, A., Briemberg, H., Bourque, P.R., Botez, S., Cashman, N., Chapman, K., Chrestian, N., Crone, M., Dobrowolski, P., Dojeiji, S., Dowling, J. J., Dupré, N., Genge, A., Gonorazky, H., Grant, I., Hasal, S., Izenberg, A., Kalra, S., Katzberg, H., Krieger, C., Leung, E., Linassi, G., Mackenzie, A., Mah, J. K., Marrero, A., Massie, R., Matte, G., McAdam, L., McMillan, H., Melanson, M., Mezei, M. M., O’Connell, C., Pfeffer, G., Phan, C., Plamondon, S., Poulin, C., Rodrigue, X., Schellenberg, K., Selby, K., Sheriko, J., Shoesmith, C., Smith, R.G., Taillon, M., Taylor, S., Venance, S., Warman-Chardon, J., Worley, S., Zinman, L., Korngut, L.
में प्रकाशित J Neuromuscul Dis (2021)
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Artigo