The Broad Phenotypic Spectrum of Aimp1-Related Disorders: Unveiling a New Case of Hereditary Spastic Paraplegia

AuthID
 P-018-DRG
6
Author(s)
Santos, M
Tipo de Documento
Abstract
Year published
2024
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 32, Páginas: 1465-1465 (1)
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Wos®
Publication Identifiers
Wos: WOS:001407868902206
Source Identifiers
ISSN: 1018-4813
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