First Pediatric Case of Autosomal Recessive Homozygotic Bestrophinopathy due to Homozygous Mutation c.187G>C p. in Two Brothers

Detalles Bibliográficos
Autores principales: Bittmann, Stefan, Luchter, Elisabeth, Villalon, Gloria, Moschuring-Alieva, Elena, Bittmann, Lara, Weissenstein, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2022
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076138/
https://www.ncbi.nlm.nih.gov/pubmed/35573931
http://dx.doi.org/10.14740/jocmr4709

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076138/
https://www.ncbi.nlm.nih.gov/pubmed/35573931
http://dx.doi.org/10.14740/jocmr4709

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