MTHFR c.604_624del ;(p.P202_E208del)

Variant ID: 1-11856419-CCTCAAAGCTCCCTGCTTCGGG-C

NM_005957.4(MTHFR):c.604_624del;(p.P202_E208del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran.

Frontiers In Pediatrics
Nejabat, Marzieh M; Inaloo, Soroor S; Sheshdeh, Afsaneh Taghipour AT; Bahramjahan, Shima S; Sarvestani, Fatima Masoomi FM; Katibeh, Pegah P; Nemati, Hamid H; Tabei, Seyed Mohammad Bagher SMB; Faghihi, Mohammad Ali MA
Publication Date: 2021

Variant appearance in text: MTHFR: 604_624del
PubMed Link: 34540776
Variant Present in the following documents:
  • Main text
  • fped-09-734946.pdf
View BVdb publication page