| pubmed-article:15508871 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C0007959 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C0442874 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C0033377 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C1847879 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C2603343 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C0205210 | lld:lifeskim |
| pubmed-article:15508871 | lifeskim:mentions | umls-concept:C0332148 | lld:lifeskim |
| pubmed-article:15508871 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:15508871 | pubmed:dateCreated | 2004-10-28 | lld:pubmed |
| pubmed-article:15508871 | pubmed:abstractText | The X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX) is a hereditary motor and sensory neuropathy linked to a variety of mutations in the connexin32 (Cx32) gene. Clinical and genetic features of CMTX have not previously been reported in Taiwanese. | lld:pubmed |
| pubmed-article:15508871 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15508871 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15508871 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15508871 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15508871 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15508871 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15508871 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:15508871 | pubmed:issn | 2072-0939 | lld:pubmed |
| pubmed-article:15508871 | pubmed:author | pubmed-author:ReidJ LJL | lld:pubmed |
| pubmed-article:15508871 | pubmed:author | pubmed-author:HuangChin-Cha... | lld:pubmed |
| pubmed-article:15508871 | pubmed:author | pubmed-author:ChuChun-CheCC | lld:pubmed |
| pubmed-article:15508871 | pubmed:author | pubmed-author:WangHung-LiHL | lld:pubmed |
| pubmed-article:15508871 | pubmed:author | pubmed-author:YuJia-MingJM | lld:pubmed |
| pubmed-article:15508871 | pubmed:author | pubmed-author:ChenJeng-Yeou... | lld:pubmed |
| pubmed-article:15508871 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15508871 | pubmed:volume | 27 | lld:pubmed |
| pubmed-article:15508871 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15508871 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15508871 | pubmed:pagination | 489-500 | lld:pubmed |
| pubmed-article:15508871 | pubmed:dateRevised | 2008-12-16 | lld:pubmed |
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| pubmed-article:15508871 | pubmed:meshHeading | pubmed-meshheading:15508871... | lld:pubmed |
| pubmed-article:15508871 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15508871 | pubmed:articleTitle | Clinical and electrophysiological studies of a family with probable X-linked dominant Charcot-Marie-Tooth neuropathy and ptosis. | lld:pubmed |
| pubmed-article:15508871 | pubmed:affiliation | First Section, Department of Neurology, Chang Gung Memorial Hospital, Taipei, Taiwan, ROC. tonywu@adm.cgmh.org.tw | lld:pubmed |
| pubmed-article:15508871 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15508871 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:2705 | entrezgene:pubmed | pubmed-article:15508871 | lld:entrezgene |
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