CP c.2050_2051del ;(p.T684Afs*6)

Variant ID: 3-148904333-CGT-C

NM_000096.3(CP):c.2050_2051del;(p.T684Afs*6)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early Diagnosis.

International Journal Of Molecular Sciences
Vila Cuenca, Marc M; Marchi, Giacomo G; Barqué, Anna A; Esteban-Jurado, Clara C; Marchetto, Alessandro A; Giorgetti, Alejandro A; Chelban, Viorica V; Houlden, Henry H; Wood, Nicholas W NW; Piubelli, Chiara C; Dorigatti Borges, Marina M; Martins de Albuquerque, Dulcinéia D; Yotsumoto Fertrin, Kleber K; Jové-Buxeda, Ester E; Sanchez-Delgado, Jordi J; Baena-Díez, Neus N; Burnyte, Birute B; Utkus, Algirdas A; Busti, Fabiana F; Kaubrys, Gintaras G; Suku, Eda E; Kowalczyk, Kamil K; Karaszewski, Bartosz B; Porter, John B JB; Pollard, Sally S; Eleftheriou, Perla P; Bignell, Patricia P; Girelli, Domenico D; Sanchez, Mayka M
Publication Date: 2020-03-30

Variant appearance in text: CP: 2050_2051delAC; Thr684Alafs*6
PubMed Link: 32235485
Variant Present in the following documents:
  • Main text
  • ijms-21-02374-s001.pdf
  • ijms-21-02374.pdf
View BVdb publication page