Cargando…
GDF6 Knockdown in a Family with Multiple Synostosis Syndrome and Speech Impairment
Multiple synostoses syndrome type 4 (SYNS4; MIM 617898) is an autosomal dominant disorder characterized by carpal-tarsal coalition and otosclerosis-associated hearing loss. SYSN4 has been associated with GDF6 gain-of-function mutations. Here we report a five-generation SYNS4 family with a reduction...
Autores principales: | Clarke, Raymond A., Fang, Zhiming, Murrell, Dedee, Sheriff, Tabrez, Eapen, Valsamma |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8470939/ https://www.ncbi.nlm.nih.gov/pubmed/34573339 http://dx.doi.org/10.3390/genes12091354 |
Ejemplares similares
-
T-Cell–Driven Fibroinflammation Inducing Follicular Dedifferentiation in Alopecia Areata and IgG4-Modified Disease
por: Kossard, Steven, et al.
Publicado: (2021) -
Conducting dermatology clinical trials during the COVID-19 pandemic
por: Sheriff, Tabrez, et al.
Publicado: (2021) -
Side effects of steroid-sparing agents in patients with bullous pemphigoid and pemphigus: A systematic review
por: Zeng, Faith A.P., et al.
Publicado: (2022) -
LRRTM4 Terminal Exon Duplicated in Family with Tourette Syndrome, Autism and ADHD
por: Clarke, Raymond A., et al.
Publicado: (2021) -
siRNA Mediate RNA Interference Concordant with Early On-Target Transient Transcriptional Interference
por: Fang, Zhiming, et al.
Publicado: (2021)