- Abstract:
-
The syndrome of benign familial infantile convulsions (BFIC) is an autosomal dominant epileptic disorder that is characterized by convulsions, with onset at age 3-12 mo and a favorable outcome. BFIC had been linked to chromosome 19q, whereas the infantile convulsions and choreoathetosis (ICCA) syndrome, in which BFIC is associated with paroxysmal dyskinesias, had been linked to chromosome 16p12-q12. BFIC appears to be frequently associated with paroxysmal dyskinesias, because many additional ...
Expand abstract - Publication status:
- Published
- Publisher copy:
- 10.1086/318805
-
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- Journal:
- American journal of human genetics
- Volume:
- 68
- Issue:
- 3
- Pages:
- 788-794
- Publication date:
- 2001-03-05
- DOI:
- EISSN:
-
1537-6605
- ISSN:
-
0002-9297
- URN:
-
uuid:510d3a2b-6a9f-4600-a9d4-84493269417f
- Source identifiers:
-
37724
- Local pid:
- pubs:37724
- Copyright date:
- 2001
Journal article
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
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