Publication
Taylor TD, Litt M, Kramer P, Pandolfo M, Angelini L, Nardocci N, Davis S, Pineda M, Hattori H, Flett PJ, Cilio MR, Bertini E, Hayflick SJ, Homozygosity mapping of Hallervorden-Spatz syndrome to chromosome 20p12.3-p13. Nat Genet14(4):479-81 1996 |
PubMed ID: 8944032 |
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Records Return:
(1)
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Catalog ID | Gender | Age at Sampling | Description | Collection_Type_id |
GM17822 | Female | 12 YR | PANTOTHENATE KINASE-ASSOCIATED NEURODEGENERATION; PKAN; HALLERVORDEN-SPATZ DISEASE INCLUDED | GM |
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