Genetics of Familial Infantile Convulsions

J Gordon Millichap

doi:10.15844/pedneurbriefs-11-11-6

Genetics of Familial Infantile Convulsions

Pediatric Neurology Briefs

Volume 11 (1997): Issue 11

By: J Gordon Millichap

Open Access

|Nov 1997

Abstract

Four families from northwestern France with autosomal dominant benign infantile convulsions and paroxysmal choreoathetosis were studied genetically by linkage analysis at the Wellcome Trust Centre for Human Genetics, University of Oxford, UK, and at Genetic Clinics in Amiens, France.

References

Szepetowski P Rochette J Berquin P Piussan C Lathrop GM Monaco AP Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16 Am J Hum Genet 1997 Oct 61 4 889 898 10.1086/514877 9382100
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DOI: https://doi.org/10.15844/pedneurbriefs-11-11-6 | Journal eISSN: 2166-6482

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Language: English

Page range: 84 - 85

Published on: Nov 1, 1997

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Benign Infantile Convulsions,

Paroxysmal Choreoathetosis,

Basal Ganglia

© 1997 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 11 (1997): Issue 11