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16061558
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http://linkedlifedata.com/resource/pubmed/id/16061558
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pubmed-article:16061558
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pubmed-article:16061558
pubmed:issue
8
lld:pubmed
pubmed-article:16061558
pubmed:dateCreated
2005-8-2
lld:pubmed
pubmed-article:16061558
pubmed:abstractText
Mutations in genes coding for the mitochondrial complex II succinate dehydrogenase (SDH) subunits cause familial neural crest derived (NCD) tumours.
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pubmed-article:16061558
pubmed:language
eng
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pubmed-article:16061558
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IM
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MEDLINE
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pubmed:month
Aug
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pubmed-article:16061558
pubmed:issn
1468-6244
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pubmed:issnType
Electronic
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pubmed-article:16061558
pubmed:volume
42
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pubmed-article:16061558
pubmed:owner
NLM
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pubmed-article:16061558
pubmed:authorsComplete
Y
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pubmed-article:16061558
pubmed:pagination
e52
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pubmed-article:16061558
pubmed:dateRevised
2008-11-20
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pubmed:year
2005
lld:pubmed
pubmed-article:16061558
pubmed:articleTitle
Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X.
lld:pubmed
pubmed-article:16061558
pubmed:affiliation
Section of Endocrinology, Department of Clinical Physiopathology, University of Florence Medical School, Florence, Italy.
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pubmed-article:16061558
pubmed:publicationType
Journal Article
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pubmed-article:16061558
pubmed:publicationType
Research Support, Non-U.S. Gov't
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