Cargando…
Erratum: Chanarin-Dorfman syndrome: Clinical report and novel mutation in ABHD5 gene
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970332/ https://www.ncbi.nlm.nih.gov/pubmed/31929317 http://dx.doi.org/10.4103/0022-3859.169758 |
Ejemplares similares
-
A New Case of Chanarin-Dorfman Syndrome with a Novel Deletion in ABHD5 Gene
por: Nakhaei, Shahrbanoo, et al.
Publicado: (2018) -
A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings
por: Eskiocak, Ali Haydar, et al.
Publicado: (2019) -
Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome
por: Tavian, Daniela, et al.
Publicado: (2021) -
A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype
por: Elsayed, Solaf Mohamed, et al.
Publicado: (2022) -
Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene
por: Redaelli, Chiara, et al.
Publicado: (2010)