Chiari malformation type I: a case-control association study of 58 developmental genes
Chiari malformation type I: a case-control association study of 58 developmental genes
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United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
Chiari malformation type I (CMI) is a disorder characterized by hindbrain overcrowding into an underdeveloped posterior cranial fossa (PCF), often causing progressive neurological symptoms. The etiology of CMI remains unclear and is most likely multifactorial. A putative genetic contribution to CMI is suggested by familial aggregation and twin stud...
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Full title
Chiari malformation type I: a case-control association study of 58 developmental genes
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TN_cdi_plos_journals_1351358899
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1351358899
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0057241
