Compound Heterozygosity in Myo5A: a Case Study of Griscelli Syndrome Type 1 with Severe Neurological Features

AuthID
 P-018-H20
5
Author(s)
Malato, MT
·
Morais, B
·
Amorim, M
·
Ramos, D
Tipo de Documento
Abstract
Year published
2024
Publicado
in CRITICAL PUBLIC HEALTH, ISSN: 0958-1596
Volume: 34, Número: 1, Páginas: 63-65 (3)
Indexing
Wos®
Publication Identifiers
Wos: WOS:001444648200061
Source Identifiers
ISSN: 0958-1596
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