Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy.

Annals of neurology

Volumn 74, Issue 3, 2013, Pages 496-501

  Hitomi, Yuki ^a   Heinzen, Erin L ^b   Donatello, Simona ^b   Dahl, Hans Henrik ^b   Damiano, John A ^b   McMahon, Jacinta M ^b   Berkovic, Samuel F ^b   Scheffer, Ingrid E ^b   Legros, Benjamin ^b   Rai, Myriam ^b   Weckhuysen, Sarah ^b   Suls, Arvid ^b   De Jonghe, Peter ^b   Pandolfo, Massimo ^b   Goldstein, David B ^b   Van Bogaert, Patrick ^b   Depondt, Chantal ^b  

^a DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN TYROSINE KINASE; TNK2 PROTEIN, HUMAN;

DNA SEQUENCE; EPILEPSY; FEMALE; GENETICS; GENOTYPE; HUMAN; INFANT; MALE; MISSENSE MUTATION; MUTATION; PEDIGREE; PRESCHOOL CHILD;

CHILD, PRESCHOOL; EPILEPSY; FEMALE; GENOTYPE; HUMANS; INFANT; MALE; MUTATION; MUTATION, MISSENSE; PEDIGREE; PROTEIN-TYROSINE KINASES; SEQUENCE ANALYSIS, DNA;

EID: 84891519543     PISSN: None     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.23934     Document Type: Article

References (0)