Identification of a de novo variant in CHUK in a patient with an EEC/AEC syndrome-like phenotype and hypogammaglobulinemia

Fulltext:
177771.pdf
Embargo:
until further notice
Size:
642.1Kb
Format:
PDF
Description:
publisher's version
Publication year
2017Source
American Journal of Medical Genetics. Part A, 173, 7, (2017), pp. 1813-1820ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
CMBI
Molecular Developmental Biology
Journal title
American Journal of Medical Genetics. Part A
Volume
vol. 173
Issue
iss. 7
Page start
p. 1813
Page end
p. 1820
Subject
Molecular Developmental BiologyThis item appears in the following Collection(s)
- Academic publications [204859]
- Electronic publications [103204]
- Faculty of Medical Sciences [81031]
- Faculty of Science [32287]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.