Output details
1 - Clinical Medicine
University of Leeds
Article title
Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects
Type
D - Journal article
Title of journal
Human Molecular Genetics
Article number
-
Volume number
22
Issue number
7
First page of article
1358
ISSN of journal
1460-2083
Year of publication
2013
URL
-
Number of additional authors
6
Additional information
"The author made a substantial contribution to the conception and design of the study"
"The author made a substantial contribution to the organisation and conduct of the study"
"The author made a substantial contribution to analysis and interpretation of study data"
"The author helped draft the output"
"The author helped critique the output for important intellectual content"
Interdisciplinary
-
Cross-referral requested
-
Research group
B - Genes and Development
Citation count
2
Proposed double-weighted
No
Double-weighted statement
-
Reserve for a double-weighted output
No
Non-English
No
English abstract
-
