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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2006-3-28
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pubmed:abstractText |
Familial tumoral calcinosis (FTC) is a rare autosomal recessive disease characterised by the development of multiple calcified masses in periarticular soft tissues; GALNT3 gene mutations have recently been described in an African American and in a Druse Arab family with FTC.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-10379593,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-12136348,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-12239638,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-15133511,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-15511669,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-15520771,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-15590700,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-15599692,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-2294551,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-2379048,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-3366131,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-8338191,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-8663203,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-8854587,
http://linkedlifedata.com/resource/pubmed/commentcorrection/16567474-9253620
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0021-9746
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
59
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
440-2
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:16567474-Autoimmune Diseases,
pubmed-meshheading:16567474-Calcinosis,
pubmed-meshheading:16567474-Child,
pubmed-meshheading:16567474-Codon, Nonsense,
pubmed-meshheading:16567474-European Continental Ancestry Group,
pubmed-meshheading:16567474-Humans,
pubmed-meshheading:16567474-Italy,
pubmed-meshheading:16567474-Lithiasis,
pubmed-meshheading:16567474-Male,
pubmed-meshheading:16567474-N-Acetylgalactosaminyltransferases,
pubmed-meshheading:16567474-Neoplasm Proteins,
pubmed-meshheading:16567474-Pedigree,
pubmed-meshheading:16567474-Testicular Diseases
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pubmed:year |
2006
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pubmed:articleTitle |
Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family.
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pubmed:affiliation |
Paediatric Department, University of Turin, Turin, Italy.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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