PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome

Heron, SE (author)

Grinton, BE (author)

Kivity, S (author)

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Afawi, Z (author)

Zuberi, SM (author)

Hughes, JN (author)

Pridmore, C (author)

Hodgson, BL (author)

Iona, X (author)

Sadleir, LG (author)

Pelekanos, J (author)

Herlenius, E (author)

Karolinska Institutet

Goldberg-Stern, H (author)

Bassan, H (author)

Haan, E (author)

Korczyn, AD (author)

Gardner, AE (author)

Corbett, MA (author)

Gecz, J (author)

Thomas, PQ (author)

Mulley, JC (author)

Berkovic, SF (author)

Scheffer, IE (author)

Dibbens, LM (author)

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 (creator_code:org_t)

Elsevier BV, 2012

2012

English.

In: American journal of human genetics. - : Elsevier BV. - 1537-6605 .- 0002-9297. ; 90:1, s. 152-160

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• Journal article (peer-reviewed)