학술논문

Case report: Revealing the rare--a Brody Disease patient from Turkey expanding the phenotype.
Document Type
Article
Source
Frontiers in Genetics; 2023, p1-11, 11p
Subject
DELAYED diagnosis
MUSCLE weakness
CREATINE kinase
PATIENTS' families
MISSENSE mutation
ARACHNOID cysts
Language
ISSN
16648021
Abstract
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