Dominantly Inherited Nemaline Myopathy
Abstract
A locus on chromosome 15q21-23 for a dominantly inherited nemaline myopathy with core-like lesions is reported in two unrelated families evaluated at University Medical Center, Nijmegen, The Netherlands.
DOI: https://doi.org/10.15844/pedneurbriefs-17-8-8 | Journal eISSN: 2166-6482
Language: English
Page range: 63 - 63
Published on: Aug 1, 2003
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2003 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.