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Spinocerebellar ataxia type 17: Report of a family with reduced penetrance of an unstable Gln49TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis…

Overview of attention for article published in BMC Medical Genomics, July 2005
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Title
Spinocerebellar ataxia type 17: Report of a family with reduced penetrance of an unstable Gln49TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypes
Published in
BMC Medical Genomics, July 2005
DOI 10.1186/1471-2350-6-27
Pubmed ID
Authors

Christine Zühlke, Andreas Dalski, Eberhard Schwinger, Ulrich Finckh

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 36 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Japan 1 3%
Turkey 1 3%
Unknown 34 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 31%
Student > Ph. D. Student 6 17%
Professor > Associate Professor 4 11%
Student > Doctoral Student 3 8%
Student > Bachelor 3 8%
Other 3 8%
Unknown 6 17%
Readers by discipline Count As %
Medicine and Dentistry 12 33%
Agricultural and Biological Sciences 9 25%
Biochemistry, Genetics and Molecular Biology 5 14%
Neuroscience 2 6%
Computer Science 1 3%
Other 0 0%
Unknown 7 19%