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.
Advisor
Publication Date
2018
Language
English
Type
Meeting Abstract
Journal Title
Journal ISSN
Volume Title
Abstract
N/A
Description
Source:
European Journal of Human Genetics
Publisher:
Nature Publishing Group
Keywords:
Subject
Biochemistry, Molecular Biology, Genetics, Heredity