학술논문

Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice-site and Charcot-Marie-Tooth phenotype with early onset symptoms
Document Type
Article
Author
Cassini, T.A.Duncan, L.Rives, L.C.Phillips, J.A.Koziura, M.E.Brault, J.Hamid, R.Cogan, J.Newman, J.H.J Adams, C.R Adams, D.E Alejandro, M.Allard, P.A Ashley, E.S Azamian, M.A Bacino, C.Balasubramanyam, A.Barseghyan, H.H Beggs, A.J Bellen, H.A Bernstein, J.P Bick, D.L Birch, C.E Boone, B.L Bostwick, B.C Briere, L.M Brown, D.Brush, M.A Burke, E.C Burrage, L.R Chao, K.Chen, S.D Clark, G.M Cooper, C.J Craigen, W.Davids, M.G Dayal, J.C Dell'Angelica, E.U Dhar, S.M Dipple, K.A Donnell-Fink, L.Dorrani, N.C Dorset, D.D Draper, D.M Dries, A.J Eckstein, D.T Emrick, L.M Eng, C.Esteves, C.Estwick, T.G Fisher, P.S Frisby, T.Frost, K.A Gahl, W.Gartner, V.A Godfrey, R.Goheen, M.A Golas, G.B Goldstein, D.G Gordon, M.E Gould, S.F Gourdine, J.-P.H Graham, B.A Groden, C.L Gropman, A.E Hackbarth, M.Haendel, M.A Hanchard, N.H Handley, L.Hardee, I.R Herzog, M.A Holm, I.M Howerton, E.J Jacob, H.Jain, M.Jiang, Y.-H.M Johnston, J.L Jones, A.E Koehler, A.M Koeller, D.S Kohane, I.N Kohler, J.M Krasnewich, D.L Krieg, E.B Krier, J.E Kyle, J.R Lalani, S.Latham, L.L Latour, Y.Lau, C.C.Lazar, J.H Lee, B.Lee, H.R Lee, P.E Levy, S.J Levy, D.A Lewis, R.P Liebendorfer, A.A Lincoln, S.Loscalzo, J.L Maas, R.F Macnamara, E.A MacRae, C.V Maduro, V.V Malicdan, M.C.A Mamounas, L.A Manolio, T.C Markello, T.Mazur, P.J McCarty, A.McConkie-Rosell, A.T McCray, A.O Metz, T.Might, M.M Moretti, P.J Mulvihill, J.L Murphy, J.M Muzny, D.E Nehrebecky, M.F Nelson, S.Scott Newberry, J.K Nicholas, S.Novacic, D.S Orange, J.Carl Pallais, J.S Palmer, C.C Papp, J.M Pena, L.E Posey, J.H Postlethwait, J.Potocki, L.N Pusey, B.B Ramoni, R.H Rodan, L.A Rosenfeld, J.Sadozai, S.L Samson, S.E Schaffer, K.Schoch, K.C Schroeder, M.A Scott, D.Sharma, P.Shashi, V.K Silverman, E.S Sinsheimer, J.G Soldatos, A.C Spillmann, R.Splinter, K.M Stoler, J.Stong, N.A Strong, K.A Sullivan, J.A Sweetser, D.P Thomas, S.J Tifft, C.J Tolman, N.Toro, C.A Tran, A.K Urv, T.M Valivullah, Z.Vilain, E.P Vogel, T.M Waggott, D.E Wahl, C.M Walley, N.A Walsh, C.F Wangler, M.A Ward, P.M Waters, K.M Webb-Robertson, B.-J.A Weech, A.Westerfield, M.T Wheeler, M.L Wise, A.A Wolfe, L.A Worthey, E.Yamamoto, S.Yang, Y.Yu, G.Zhang, J.A Zornio, P.
Source
In: Molecular Genetics and Genomic Medicine. (Molecular Genetics and Genomic Medicine, June 2019, 7(6))
Subject
Language
English
ISSN
23249269