Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
about
Immune and myodegenerative pathomechanisms in inclusion body myositisProteomics of rimmed vacuoles define new risk allele in inclusion body myositis.Sporadic inclusion body myositis - a myodegenerative disease or an inflammatory myopathy.Association study reveals novel risk loci for sporadic inclusion body myositis.Genetics in inclusion body myositis.TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.
P2860
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 08 August 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
@en
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
@nl
type
label
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
@en
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
@nl
prefLabel
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
@en
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
@nl
P2093
P2860
P50
P1476
Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
@en
P2093
Alan M Pittman
Aziz Shaibani
Boel De Paepe
Christina Liang
Conceição Bettencourt
David Hilton-Jones
Deborah Hughes
Edmar Zanoteli
Estelle Healy
Henry Houlden
P2860
P304
218.e1-218.e9
P356
10.1016/J.NEUROBIOLAGING.2016.07.024
P577
2016-08-08T00:00:00Z