A Mild Case of Jeune Syndrome Associated with a Recurrent Missense Variant in DYNC2H1: Confirmation of a Genotype-Phenotype Correlation.
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Publisher DOI
PubMed ID
38224688
Date of Publication
2024-02
Publication Type
Article
Subject(s)
Language(s)
en
Contributor(s)
Usemann, Jakob |
Series
Klinische Pädiatrie
Publisher
Thieme
ISSN
1439-3824
Access(Rights)
metadata.only