K. R. Vanmolkot

Childhood epilepsy, familial hemiplegic migraine, cerebellar ataxia, and a new CACNA1A mutation

M. Ferrari, R. Flink, R. Raininko, 2004, Neurology.

Migraine genetics: An update

M. Ferrari, R. Frants, A. M. Maagdenberg, 2005, Current pain and headache reports.

Migraine genetics : from monogenic to complex forms

K. Vanmolkot, K. R. Vanmolkot, 2008 .

p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation.

M. Bamshad, R. Tenconi, H. Brunner, 2001, American journal of human genetics.

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

A. Palotie, R. Frants, M. Wessman, 2004, Neurogenetics.

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.

H. Brunner, F. McKeon, J. McGrath, 2001, Human molecular genetics.

Alternating Hemiplegia of Childhood: No Mutations in the Glutamate Transporter EAAT1

M. Ferrari, H. Stroink, B. de Vries, 2006, Neuropediatrics.

Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63.

E. Krieger, H. Brunner, F. McKeon, 2002, Human molecular genetics.