CSMD1 c.818+89088C>T

Variant ID: 8-3766337-G-A

NM_033225.5(CSMD1):c.818+89088C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Whole-genome sequencing in an autism multiplex family.

Molecular Autism
Shi, Lingling L; Zhang, Xu X; Golhar, Ryan R; Otieno, Frederick G FG; He, Mingze M; Hou, Cuiping C; Kim, Cecilia C; Keating, Brendan B; Lyon, Gholson J GJ; Wang, Kai K; Hakonarson, Hakon H
Publication Date: 2013-04-18

Variant appearance in text: rs2930372
PubMed Link: 23597238
Variant Present in the following documents:
  • Main text
  • 2040-2392-4-8.pdf
View BVdb publication page