Dejerine-Sottas disease in childhood-Genetic and sonographic heterogeneity-Reference-Cited by-同舟云学术

Dejerine-Sottas disease in childhood-Genetic and sonographic heterogeneity

Published:2018-02-21 Issue:4 Volume:8 Page:e00919
ISSN:2162-3279
Container-title:Brain and Behavior
language:en
Short-container-title:Brain Behav

Author:

Hobbelink Sanne M. R.¹,Brockley Cain R.²,Kennedy Rachel A.³⁴,Carroll Kate³⁴,de Valle Katy³⁴,Rao Padma²,Davis Mark R.⁵,Laing Nigel G.⁵⁶,Voermans Nicol C.¹,Ryan Monique M.³⁴⁷,Yiu Eppie M.³⁴⁷^ORCID

Affiliation:

1. Neurology Department; Radboud University Medical Center; Nijmegen The Netherlands

2. Medical Imaging Department; The Royal Children's Hospital Melbourne; Parkville Vic. Australia

3. Neurology Department; The Royal Children's Hospital Melbourne; Parkville Vic. Australia

4. Neurosciences Research; Murdoch Childrens Research Institute; Parkville Vic. Australia

5. Neurogenetics Unit; Department of Diagnostic Genomics; PathWest Laboratory Medicine; QEII Medical Centre; Nedlands WA Australia

6. QEII Medical Centre; Centre for Medical Research University of Western Australia and Harry Perkins Institute of Medical Research; Nedlands WA Australia

7. Department of Paediatrics; The University of Melbourne; Parkville Vic. Australia

Funder

National Health and Medical Research Council

Prinses Beatrix Spierfonds

Publisher

Wiley

Subject

Behavioral Neuroscience

Reference15 articles.

1. Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1;Abe;Journal of Human Genetics,2010

2. Compound heterozygous deletions of PMP22 causing severe Charcot-Marie-Tooth disease of the Dejerine-Sottas disease phenotype;Al-Thihli;American Journal of Medical Genetics. Part A,2008

3. Genetic spectrum of hereditary neuropathies with onset in the first year of life;Baets;Brain,2011