Missing/wrong data?
Log in to edit
Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings
scientific article published on 29 April 2011
Author/s
author: Malte Spielmann, Eva Klopocki, Stefan Mundlos, Denise Horn
Work details
Publication date
April 29, 2011
-
-
Language
English
Copyright status
Copyright status information is not available for this work. The copyright status depends on the jurisdiction, the author's date of death and the date the work was created or published.
To learn more about copyright terms in different countries, visit the countries and terms page.