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BDNF c.31_33delinsCAT ;(p.S11H)
Variant ID: 11-27680079-TGA-ATG
NM_001709.4(
BDNF
):c.31_33delinsCAT;(p.S11H)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Neuron type-specific increase in lamin B1 contributes to nuclear dysfunction in Huntington's disease.
Embo Molecular Medicine
Alcalá-Vida, Rafael R; Garcia-Forn, Marta M; Castany-Pladevall, Carla C; Creus-Muncunill, Jordi J; Ito, Yoko Y; Blanco, Enrique E; Golbano, Arantxa A; Crespí-Vázquez, Kilian K; Parry, Aled A; Slater, Guy G; Samarajiwa, Shamith S; Peiró, Sandra S; Di Croce, Luciano L; Narita, Masashi M; Pérez-Navarro, Esther E
Publication Date: 2021-02-05
Variant appearance in text: BDNF: S11H
PubMed Link:
33369245
Variant Present in the following documents:
Main text
EMMM-13-e12105.pdf
View BVdb publication page