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Cerebral cavernous malformation: Clinical report of two families with variable phenotype associated with KRIT1 mutation

✍ Scribed by Balasubramanian, Meena; Jain, Vani; Glover, Rhona C.; Robertson, Lisa K.; Mordekar, Santosh R.

Book ID: 122100472
Publisher: Elsevier Science
Year: 2013
Tongue: English
Weight: 569 KB
Volume: 17
Category: Article
ISSN: 1090-3798
DOI: 10.1016/j.ejpn.2013.05.003

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