CCM1 gene deletion identified by MLPA in cerebral cavernous malformation

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Neurosurgical Review, Vol. 30, Iss. 2, 2007-04 ,pp. : 155-160

Springer Publishing Company

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Study of cerebral cavernous malformation in Spain and Portugal: High prevalence of a 14 bp deletion in exon 5 of MGC4607 (CCM2 gene)

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Journal of Neurology, Vol. 254, Iss. 3, 2007-03 ,pp. : 322-326

Springer Publishing Company

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Clinical impact of CCM mutation detection in familial cavernous angioma

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Child's Nervous System, Vol. 22, Iss. 11, 2006-11 ,pp. : 1461-1464

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Cutaneous Venous Malformations Related to KRIT1 Mutation: Case Report and Literature Review

By Grippaudo Francesca   Piane Maria   Amoroso Matteo   Longo Benedetto   Penco Silvana   Chessa Luciana   Giubettini Maria   Santanelli Fabio  

Journal of Molecular Neuroscience, Vol. 51, Iss. 2, 2013-10 ,pp. : 442-445

Humana Press, Inc

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Familial cerebral cavernous malformations associated with a splice-site CCM2 deletion

By Jiménez-Huete Adolfo  

Journal of Neurology, Vol. 256, Iss. 1, 2009-01 ,pp. : 137-138

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