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PDCD10 gene mutations in multiple cerebral cavernous malformations

PDCD10 gene mutations in multiple cerebral cavernous malformations

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1618141425

PDCD10 gene mutations in multiple cerebral cavernous malformations

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Publication information

Publisher

United States: Public Library of Science

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Scope and Contents

Contents

Cerebral cavernous malformations (CCMs) are vascular abnormalities that may cause seizures, intracerebral haemorrhages, and focal neurological deficits. Familial form shows an autosomal dominant pattern of inheritance with incomplete penetrance and variable clinical expression. Three genes have been identified causing familial CCM: KRIT1/CCM1, MGC4...

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Full title

PDCD10 gene mutations in multiple cerebral cavernous malformations

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Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1618141425

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1618141425

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0110438

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