NPC1 c.1655-785A>C

Variant ID: 18-21128857-T-G

NM_000271.4(NPC1):c.1655-785A>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


An uncommon inheritance pattern in Niemann-Pick disease type C: identification of probable paternal germline mosaicism in a Mexican family.

Bmc Neurology
Cervera-Gaviria, Marivi M; Alcántara-Ortigoza, Miguel Angel MA; González-Del Angel, Ariadna A; Moyers-Pérez, Paola P; Legorreta-Ramírez, Blanca Gabriela Lizet BG; Barrera-Carmona, Nancy N; Cervera-Gaviria, Jaime J
Publication Date: 2016-08-22

Variant appearance in text: rs1652344
PubMed Link: 27549128
Variant Present in the following documents:
  • Main text
  • 12883_2016_Article_649.pdf
View BVdb publication page