Molecular Analysis of PKU-Associated PAH Mutations: A Fast and Simple Genotyping Test

Neonatal screening for phenylketonuria (PKU, OMIM: 261600) was introduced at the end of the 1960s. We developed a rapid and simple molecular test for the most frequent phenylalanine hydroxylase (PAH, Gene ID: 5053) mutations. Using this method to detect the 18 most frequent mutations, it is possible...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado en:Methods Protoc
Autores principales: Tolve, Manuela, Artiola, Cristiana, Pasquali, Amelia, Giovanniello, Teresa, D’Amici, Sirio, Angeloni, Antonio, Pizzuti, Antonio, Carducci, Claudia, Leuzzi, Vincenzo, Carducci, Carla
Formato: Artigo
Lenguaje:Inglês
Publicado: MDPI 2018
Materias:
Technical Note
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6481045/
https://ncbi.nlm.nih.gov/pubmed/31164572
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/mps1030030
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Ejemplares similares