Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures

Authors :: Heron, S.E.
Cox, K.
Grinton, B.E.
Zuberi, S.M.
Kivity, S.
Afawi, Z.
Straussberg, R.
Berkovic, S.F.
Scheffer, I.E.
Mulley, J.C.
Source :: Journal of Medical Genetics. Dec, 2007, Vol. 44 Issue 12, p791, 6 p.
Publication Year :: 2007

Subjects :: Convulsions -- Causes of
Convulsions -- Demographic aspects
Potassium channels -- Genetic aspects
Potassium channels -- Health aspects
Familial diseases -- Genetic aspects
Familial diseases -- Research
Gene mutations -- Health aspects
Infants (Newborn) -- Diseases
Infants (Newborn) -- Research
Health

Tools