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Author/Creator Zuchner, Stephan

21. O3–01–04: The identification of rare variants in late‐onset Alzheimer's disease using extended families. (1st July 2013)

Authors:
Kohli, Martin; Kunkle, Brian; Naj, Adam; Carney, Regina M.; Hamilton‐Nelson, Kara; Rolati, Sophie; Whitehead, Patrice L.; Gilbert, John; Martin, Eden; Beecham, Gary; Wang, Li‐San; Mayeux, Richard; Haines, Jonathan; Farrer, Lindsay; Schellenberg, Gerard; Zuchner, Stephan; Pericak‐Vance, Margaret
Journal:
Alzheimer's & dementia
Issue:
Volume 9:Supplement 4S(2013)Part 13
Page Start:
P518
Record Type:
Journal Article
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23. Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation. (23rd March 2015)

Authors:
Jerath, Nivedita U.; Crockett, Cameron D.; Moore, Steven A.; Shy, Michael E.; Weihl, Conrad C.; Chou, Tsui-Fen; Grider, Tiffany; Gonzalez, Michael A.; Zuchner, Stephan; Swenson, Andrea
Other Names:
Morrison Patrick Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2015(2015)
Page Start:
Record Type:
Journal Article
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24. Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation. (23rd March 2015)

Authors:
Jerath, Nivedita U.; Crockett, Cameron D.; Moore, Steven A.; Shy, Michael E.; Weihl, Conrad C.; Chou, Tsui-Fen; Grider, Tiffany; Gonzalez, Michael A.; Zuchner, Stephan; Swenson, Andrea
Other Names:
Morrison Patrick Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2015(2015)
Page Start:
Record Type:
Journal Article
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25. Reply: The p.Ser107Leu in BICD2 is a mutation 'hot spot' causing distal spinal muscular atrophy. (10th June 2015)

Authors:
Rossor, Alexander M.; Oates, Emily C.; Salter, Hannah K.; Liu, Yang; Murphy, Sinead M.; Schule, Rebecca; Gonzales, Michael A.; Scoto, Mariacristina; Phadke, Rahul; Sewry, Caroline A.; Houlden, Henry; Jordanova, Albena; Tournev, Iyailo; Chamova, Teodora; Litvinenko, Ivan; Zuchner, Stephan; Herrman...
Journal:
Brain
Issue:
Volume 138:Part 11(2015:Nov.)
Page Start:
e392
Record Type:
Journal Article
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