Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Rossor, Alexander M.; Oates, Emily C.; Salter, Hannah K.; Liu, Yang; Murphy, Sinead M.; Schule, Rebecca; Gonzalez, Michael A.; Scoto, Mariacristina; Phadke, Rahul; Sewry, Caroline A.; Houlden, Henry; Jordanova, Albena; Tournev, Iyailo; Chamova, Teodora; Litvinenko, Ivan; Zuchner, Stephan; Herrmann, David N.; Blake, Julian; Sowden, Janet E.; Acsadi, Gyuda; Rodriguez, Michael L.; Menezes, Manoj P.; Clarke, Nigel F.; Grumbach, Michaela Auer; Bullock, Simon L.; Muntoni, Francesco; Reilly, Mary M.; North, Kathryn N.

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Autor(en):

Rossor, Alexander M.; Oates, Emily C.; Salter, Hannah K.; Liu, Yang; Murphy, Sinead M.; Schule, Rebecca; Gonzalez, Michael A.; Scoto, Mariacristina; Phadke, Rahul; Sewry, Caroline A.; Houlden, Henry; Jordanova, Albena; Tournev, Iyailo; Chamova, Teodora; Litvinenko, Ivan; Zuchner, Stephan; Herrmann, David N.; Blake, Julian; Sowden, Janet E.; Acsadi, Gyuda; Rodriguez, Michael L.; Menezes, Manoj P.; Clarke, Nigel F.; Grumbach, Michaela Auer; Bullock, Simon L.; Muntoni, Francesco; Reilly, Mary M.; North, Kathryn N.

Tübinger Autor(en):

Schüle-Freyer, Rebecca

Erschienen in:

Brain (2015), Bd. 138, S. 293-310

Verlagsangabe:

Oxford Univ Press

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1093/brain/awu356

ISSN:

0006-8950