Genomic

Dataset Information

Spinocerebellar Ataxias Natural History


ABSTRACT:

Spinocerebellar ataxias (SCA) are genetic neurological diseases that cause imbalance, poor coordination, and speech difficulties. There are different kinds of SCA and this study will focus on types 1, 2, 3, and 6 (SCA 1, SCA 2, SCA 3, also known as Machado-Joseph disease and SCA 6). The diseases are rare, slowly progressive, cause increasingly severe neurological difficulties and are variable across and within genotypes. The purpose of this research study is to bring together a group of experts in the field of SCA for the purpose of learning more about the disease.

The research questions are:

  • How does the disease progress over time?
  • What are the best ways to measure disease progression?
  • Do some genes, other than the gene that is abnormal in the SCA disease, have any effect on the way the disease behaves?

PROVIDER: phs001332 | dbGaP |

SECONDARY ACCESSION(S): PRJNA378822PRJNA378821

REPOSITORIES: dbGaP

Dataset's files

Source:
Action DRS
GapExchange_phs001332.v1.p1.xml Xml
dbGaPEx2.1.5.xsd Other
phs001332.v1-Documents.zip Other
Study_Report.phs001332.CRC_SCA_7301.v1.p1.MULTI.pdf Pdf
manifest_phs001332.CRC_SCA_7301.v1.p1.c1.GRU-IRB-PUB.pdf Pdf
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