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Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant? (2021)

First Author: Yau WY

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/acn3.51330

PubMed Identifier: 33780167

Publication URI: http://europepmc.org/abstract/MED/33780167

Type: Journal Article/Review

Volume: 8

Parent Publication: Annals of clinical and translational neurology

Issue: 4

ISSN: 2328-9503