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Author/Creator Alcaraz, Wendy A.

1. A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia. Issue 4 (9th September 2016)

Authors:
Helbig, Katherine L.; Hedrich, Ulrike B.S.; Shinde, Deepali N.; Krey, Ilona; Teichmann, Anne‐Christin; Hentschel, Julia; Schubert, Julian; Chamberlin, Adam C.; Huether, Robert; Lu, Hsiao‐Mei; Alcaraz, Wendy A.; Tang, Sha; Jungbluth, Chelsy; Dugan, Sarah L.; Vainionpää, Leena; Karle, Kathrin N.; S...
Journal:
Annals of neurology
Issue:
Volume 80:Issue 4(2016:Oct.)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Deficiency of WARS2, encoding mitochondrial tryptophanyl tRNA synthetase, causes severe infantile onset leukoencephalopathy. Issue 9 (26th June 2017)

Authors:
Theisen, Benjamin E.; Rumyantseva, Anastasia; Cohen, Julie S.; Alcaraz, Wendy A.; Shinde, Deepali N.; Tang, Sha; Srivastava, Siddarth; Pevsner, Jonathan; Trifunovic, Aleksandra; Fatemi, Ali
Journal:
American journal of medical genetics
Issue:
Volume 173:Issue 9(2017)
Page Start:
2505
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗