Publication: A new recognizable recessive syndrome with distinct dysmorphism, lymphedema and sensorineural hearing loss caused by carboxypeptidase D mutations
Program
KU-Authors
KU Authors
Co-Authors
Altunoğlu, U.
Laupheimer, S.
Bonnard, C.
Editor & Affiliation
Compiler & Affiliation
Translator
Other Contributor
Date
Language
Type
Embargo Status
N/A
Journal Title
Journal ISSN
Volume Title
Alternative Title
Abstract
BAKILACAK
Source
Publisher
Nature Publishing Group
Subject
Biochemistry, Molecular Biology, Genetics, Heredity
Citation
Has Part
Source
European Journal of Human Genetics
Book Series Title
Edition
DOI
item.page.datauri
Link
Rights
N/A