Arg953 mutation in Periaxin causes CMT4F without nerve hypertrophy on ultrasound imaging: A case report and review of the literature

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Bibliographic Details
Published inClinical neurophysiology Vol. 147; pp. 14 - 16
Main Authors Castoro, Ryan, Caress, James B., Li, Jun, Cartwright, Michael S.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.03.2023
Subjects
Hereditary Sensory and Motor Neuropathy
Humans
Hypertrophy
Membrane Proteins - genetics
Mutation
Neurology
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ISSN1388-2457
1872-8952
1872-8952
DOI10.1016/j.clinph.2022.12.007

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Bibliography:ObjectType-Case Study-3
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ObjectType-Correspondence-4
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ObjectType-Review-1
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ISSN:1388-2457
1872-8952
1872-8952
DOI:10.1016/j.clinph.2022.12.007