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| pubmed-article:9150176 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:9150176 | pubmed:dateCreated | 1997-6-3 | lld:pubmed |
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| pubmed-article:9150176 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:9150176 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9150176 | pubmed:month | May | lld:pubmed |
| pubmed-article:9150176 | pubmed:issn | 0002-9297 | lld:pubmed |
| pubmed-article:9150176 | pubmed:author | pubmed-author:AshizawaTT | lld:pubmed |
| pubmed-article:9150176 | pubmed:author | pubmed-author:PatelP IPI | lld:pubmed |
| pubmed-article:9150176 | pubmed:author | pubmed-author:BidichandaniS... | lld:pubmed |
| pubmed-article:9150176 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9150176 | pubmed:volume | 60 | lld:pubmed |
| pubmed-article:9150176 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9150176 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9150176 | pubmed:pagination | 1251-6 | lld:pubmed |
| pubmed-article:9150176 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:9150176 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9150176 | pubmed:articleTitle | Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion. | lld:pubmed |
| pubmed-article:9150176 | pubmed:publicationType | Letter | lld:pubmed |
| pubmed-article:9150176 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:9150176 | pubmed:publicationType | Case Reports | lld:pubmed |
| pubmed-article:9150176 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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