ScienceOpen:
research and publishing network
For Publishers
Discovery
Metadata
Peer review
Hosting
Publishing
For Researchers
Join
Publish
Review
Collect
My ScienceOpen
Sign in
Register
Dashboard
Blog
About
Search
Advanced search
My ScienceOpen
Sign in
Register
Dashboard
Search
Search
Advanced search
For Publishers
Discovery
Metadata
Peer review
Hosting
Publishing
For Researchers
Join
Publish
Review
Collect
Blog
About
0
views
0
references
Top references
cited by
1
Cite as...
0 reviews
Review
0
comments
Comment
0
recommends
+1
Recommend
0
collections
Add to
0
shares
Share
Twitter
Sina Weibo
Facebook
Email
903
similar
All similar
Record
: found
Abstract
: not found
Article
: not found
Merosin positive congenital muscular dystrophy with mental deficiency, epilepsy and MRI changes in the cerebral white matter
Author(s):
B Echenne
Publication date
Created:
May 1997
Publication date
(Print):
May 1997
Journal:
Neuromuscular Disorders
Publisher:
Elsevier BV
Read this article at
ScienceOpen
Publisher
Review
Review article
Invite someone to review
Bookmark
Cite as...
There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Related collections
Probing cerebral hemodynamics with BOLD fMRI
Author and article information
Journal
Title:
Neuromuscular Disorders
Abbreviated Title:
Neuromuscular Disorders
Publisher:
Elsevier BV
ISSN (Print):
09608966
Publication date Created:
May 1997
Publication date (Print):
May 1997
Volume
: 7
Issue
: 3
Pages
: 187-190
Article
DOI:
10.1016/S0960-8966(97)00452-5
SO-VID:
e1c829c1-b797-4d77-ab43-1741891707b5
Copyright ©
© 1997
License:
https://www.elsevier.com/tdm/userlicense/1.0/
History
Data availability:
Comments
Comment on this article
Sign in to comment
scite_
Similar content
903
Laminin-α2 Chain (Merosin M) is Preserved in the Walker-Warburg Syndrome
Authors:
SŞ. Kükner
,
Y Gürer
,
I Saatci
…
An atypical case of partial merosin deficiency congenital muscular dystrophy.
Authors:
G Scarlato
,
A Prelle
,
G. P. Comi
…
Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
Authors:
Dominique Hillaire
,
Anne Leclerc
,
Sabine Fauré
…
See all similar
Cited by
1
Congenital Muscular Dystrophies
Authors:
See all cited by