| pubmed-article:9100224 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0002986 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0002268 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0031437 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0079429 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0439658 | lld:lifeskim |
| pubmed-article:9100224 | lifeskim:mentions | umls-concept:C0439858 | lld:lifeskim |
| pubmed-article:9100224 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:9100224 | pubmed:dateCreated | 1997-7-21 | lld:pubmed |
| pubmed-article:9100224 | pubmed:abstractText | Fabry disease, an X-linked inborn error of glycosphingolipid catabolism, results from mutations in the alpha-galactosidase A (alpha-Gal A) gene located at Xq22.1. To determine the nature and frequency of the molecular lesions causing the classical and milder variant Fabry phenotypes and for precise carrier detection, the alpha-Gal A lesions in 42 unrelated Fabry hemizygotes were determined. | lld:pubmed |
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| pubmed-article:9100224 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9100224 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9100224 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:9100224 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9100224 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:9100224 | pubmed:issn | 1076-1551 | lld:pubmed |
| pubmed-article:9100224 | pubmed:author | pubmed-author:DesnickR JRJ | lld:pubmed |
| pubmed-article:9100224 | pubmed:author | pubmed-author:D'SouzaMM | lld:pubmed |
| pubmed-article:9100224 | pubmed:author | pubmed-author:GeeA HAH | lld:pubmed |
| pubmed-article:9100224 | pubmed:author | pubmed-author:EnriquezA LAL | lld:pubmed |
| pubmed-article:9100224 | pubmed:author | pubmed-author:BurgertT STS | lld:pubmed |
| pubmed-article:9100224 | pubmed:author | pubmed-author:AshleyG AGA | lld:pubmed |
| pubmed-article:9100224 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9100224 | pubmed:volume | 3 | lld:pubmed |
| pubmed-article:9100224 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9100224 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9100224 | pubmed:pagination | 174-82 | lld:pubmed |
| pubmed-article:9100224 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:9100224 | pubmed:meshHeading | pubmed-meshheading:9100224-... | lld:pubmed |
| pubmed-article:9100224 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9100224 | pubmed:articleTitle | Fabry disease: thirty-five mutations in the alpha-galactosidase A gene in patients with classic and variant phenotypes. | lld:pubmed |
| pubmed-article:9100224 | pubmed:affiliation | Department of Human Genetics, Mount Sinai School of Medicine, New York, NY 10029, USA. | lld:pubmed |
| pubmed-article:9100224 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9100224 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:9100224 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:2717 | entrezgene:pubmed | pubmed-article:9100224 | lld:entrezgene |
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