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Figure 1 | BMC Neurology

Figure 1

From: Severe and rapidly progressing cognitive phenotype in a SCA17-family with only marginally expanded CAG/CAA repeats in the TATA-box binding protein gene: A case report

Figure 1

Pedigree of the SCA17 family. Individuals marked with solid black have a molecular diagnosis of SCA17 accompanied by clinical manifestations of neurological disorders. Individuals marked with gray shading have a clinical diagnosis of a neurological disorder, which has not been confirmed on the molecular level. The proband is marked by an arrow.

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BMC Neurology

ISSN: 1471-2377

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