Nalaganje...

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.

Benign infantile familial convulsions is an autosomal dominant disorder characterized by nonfebrile seizures, with the first attack occurring at age 3-12 mo. It is one of the rare forms of epilepsy that are inherited as monogenic Mendelian traits, thus providing a powerful tool for mapping genes inv...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Szepetowski, P, Rochette, J, Berquin, P, Piussan, C, Lathrop, G M, Monaco, A P
Format: Artigo
Jezik:Inglês
Izdano: 1997
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715981/
https://ncbi.nlm.nih.gov/pubmed/9382100
Oznake: Označite
Brez oznak, prvi označite!