학술논문
Quantification of dysarthrοphonia in a Cypriot family with autosomal recessive hereditary spastic paraplegia associated with a homozygous SPG11 mutation.
Document Type
Journal Article
Source
Subject
*NEURODEGENERATION
*MOLECULAR genetics
*GENETIC testing
*SPINAL cord
*MEDICAL genetics
*PATIENTS
*FAMILIES
*GLOTTIS
*GENETIC mutation
*PROTEINS
*SPEECH disorders
*GENETIC carriers
*FAMILIAL spastic paraplegia
*GENOTYPES
PHYSIOLOGICAL aspects of speech
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Language
ISSN
1590-1874
Abstract