F13A1 c.320-2256C>A

Variant ID: 6-6269298-G-T

NM_000129.3(F13A1):c.320-2256C>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency.

International Journal Of Hematology-Oncology And Stem Cell Research
Shahraki, Hojat H; Dorgalaleh, Akbar A; Fathi, Majid M; Tabibian, Shadi S; Teimourian, Shahram S; Mollanoori, Hasan H; Khiabani, Alireza A; Zaker, Farhad F
Publication Date: 2020-10-01

Variant appearance in text: rs4960181
PubMed Link: 33603988
Variant Present in the following documents:
  • Main text
  • IJHOSCR-14-265.pdf
View BVdb publication page