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Further description of the phenotypic spectrum of neuronal ceroid lipofuscinosis type 11. (2025)

First Author: Nóbrega PR

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/10.1016/j.gim.2024.101291

PubMed Identifier: 39394881

Publication URI: http://europepmc.org/abstract/MED/39394881

Type: Journal Article/Review

Volume: 27

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 1

ISSN: 1098-3600