GAA c.692+3G>C

Variant ID: 17-78079696-G-C

NM_000152.3(GAA):c.692+3G>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Newborn Screening for Pompe Disease: Pennsylvania Experience.

International Journal Of Neonatal Screening
Ficicioglu, Can C; Ahrens-Nicklas, Rebecca C RC; Barch, Joshua J; Cuddapah, Sanmati R SR; DiBoscio, Brenda S BS; DiPerna, James C JC; Gordon, Patricia L PL; Henderson, Nadene N; Menello, Caitlin C; Luongo, Nicole N; Ortiz, Damara D; Xiao, Rui R
Publication Date: 2020-11-13

Variant appearance in text: GAA: 692+3G>C
PubMed Link: 33202836
Variant Present in the following documents:
  • Main text
  • IJNS-06-00089.pdf
View BVdb publication page