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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Sheila A Simpson

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Brain : a Journal of Neurology|March 5, 2003

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical courseFerdinando Squitieri, Cinzia Gellera, Milena Cannella, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2018

27 years of prenatal diagnosis for Huntington disease in the United KingdomRaul E Piña-Aguilar, Sheila A Simpson, Abdulrahman Alshatti, et al.

Nature Genetics|May 5, 2015

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate exportAndrea Legati, Donatella Giovannini, Gaël Nicolas, et al.

Neurogenetics|January 22, 2013

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.

Pageof 2

Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Brain : a Journal of Neurology|March 5, 2003

Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical courseFerdinando Squitieri, Cinzia Gellera, Milena Cannella, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2018

27 years of prenatal diagnosis for Huntington disease in the United KingdomRaul E Piña-Aguilar, Sheila A Simpson, Abdulrahman Alshatti, et al.

Nature Genetics|May 5, 2015

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate exportAndrea Legati, Donatella Giovannini, Gaël Nicolas, et al.

Neurogenetics|January 22, 2013

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcificationSandy Chan Hsu, Renee L Sears, Roberta R Lemos, et al.

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