Mitochondrial DNA Mutation in Rett Syndrome

J Gordon Millichap

doi:10.15844/pedneurbriefs-12-1-8

Mitochondrial DNA Mutation in Rett Syndrome

Pediatric Neurology Briefs

Volume 12 (1998): Issue 1

By: J Gordon Millichap

Open Access

|Jan 1998

Abstract

Analysis of mitochondrial DNA from 15 children with Rett syndrome (RS) and 14 of their mothers is reported from the Department of Pediatrics, Beijing Medical University, China.

References

Tang J Qj Y Bao X-H Wu X-R Mutational analysis of mitochondrial DNA of children with Rett syndrome Pediatr Neurol 1997 Nov 17 4 327 330 10.1016/S0887-8994(97)00151-3 9436797
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Ogawa A Mitsudome A Yasumoto S Matsumoto T Japanese monozygotic twins with Rett syndrome Brain Dev 1997 Dec 19 8 568 570 10.1016/S0387-7604(97)00084-3 9440804
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-12-1-8 | Journal eISSN: 2166-6482

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Language: English

Page range: 5 - 5

Published on: Jan 1, 1998

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Mitochondrial DNA,

Rett Syndrome,

Maternal Inheritance

© 1998 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 12 (1998): Issue 1