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Cutaneous findings of familial cerebral cavernous malformation syndrome due to the common Hispanic mutation

  • Published:2020-02-26 Issue:5 Volume:182 Page:1066-1072
  • ISSN:1552-4825
  • Container-title:American Journal of Medical Genetics Part A
  • language:en
  • Short-container-title:Am J Med Genet

Author:

Manole Athanasios K.1,Forrester Vernon J.2ORCID,Zlotoff Barrett J.2,Hart Blaine L.3,Morrison Leslie A.4

Affiliation:

1. Department of Neurosurgery, Division of Physical Medicine and RehabilitationUniversity of New Mexico Albuquerque New Mexico USA

2. Department of DermatologyUniversity of Virginia Charlottesville Virginia USA

3. Department of RadiologyUniversity of New Mexico Albuquerque New Mexico USA

4. Department of NeurologyUniversity of New Mexico Albuquerque New Mexico USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Brain vascular malformation consortium: Overview, progress and future directions;Akers A.;The Journal of Rare Disorders,2013

2. Neurofibromatosis type 1

3. Progressive late‐onset of cutaneous angiomatosis as possible sign of cerebral cavernous malformations;Campione E.;Dermatology Online Journal,2013

4. Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas

5. Vascular Malformations: A Review

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