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AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range. (2022)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ejmg.2022.104620

PubMed Identifier: 36122674

Publication URI: http://europepmc.org/abstract/MED/36122674

Type: Journal Article/Review

Volume: 65

Parent Publication: European journal of medical genetics

Issue: 11

ISSN: 1769-7212