Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia
Abstract Type 2 spinal muscular atrophy with lower extremity dominance (SMALED2) is caused by bicaudal D cargo adaptor 2 (BICD2) variants. However, the SMALED2 genotype and phenotype correlation have not been thoroughly characterized. We identified de novo heterozygous BICD2 missense variants in two...
Saved in:
Main Authors: | Layla Masuda, Akihiro Hasegawa, Hiromi Kamura, Fuyuki Hasegawa, Michihiro Yamamura, Kosuke Taniguchi, Yuki Ito, Kenichiro Hata, Osamu Samura, Aikou Okamoto |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2024-08-01
|
Series: | Human Genome Variation |
Online Access: | https://doi.org/10.1038/s41439-024-00290-z |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Arthrogryposis Multiplex Congenita: Case Report
by: Ayla Aktulay, et al.
Published: (2013-12-01) -
Arthrogryposis Multiplex Congenita: Multiple Congenital Joint Contractures
by: Hamza Sucuoglu, et al.
Published: (2015-01-01) -
Conjunctival Lymphangiogenesis Was Associated with the Degree of Aggression in Substantial Recurrent Pterygia
by: Wei Zhao, et al.
Published: (2016-01-01) -
Characterization of a Small Supernumerary Marker Chromosome Derived from Xq28 and 14q11.2 Detected Prenatally
by: Akihiro Hasegawa, et al.
Published: (2018-01-01) -
Outcomes of Vertical Split Conjunctival Autograft Using Fibrin Glue in Treatment of Primary Double-Headed Pterygia
by: Tarek Roshdy Elhamaky, et al.
Published: (2018-01-01)