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Autosomal dominant vasovagal syncope: Clinical features and linkage to chromosome 15q26
K. M. Klein ,
C. J. Bromhead ,
K. R. Smith ,
C. J. O'Callaghan ,
S. J. Corcoran ,
S. E. Heron ,
X. Iona ,
B. L. Hodgson ,
J. M. McMahon ,
K. M. Lawrence ,
I. E. Scheffer ,
L. M. Dibbens ,
M. Bahlo ,
S. F. Berkovic
April 15 2013
April 15 2013
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Abstract
To establish the occurrence of an autosomal dominant form of vasovagal syncope (VVS)
by detailed phenotyping of multiplex families and identification of the causative
locus.