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PMID: 744199
Published · ppublish
English
Journal Article
Charcot-Marie-Tooth disease with sex-linked inheritance, linkage studies and abnormal serum alkaline phosphatase levels.
Abstract
A family with Charcot-Marie-Tooth disease (CMT) is described. An irregular dominant sex-linked inheritance is observed. No linkage relationship between the Xg(a) blood group locus and the CMT locus was established. Abnormal values of the serum alkaline phosphatase level were found in affected and unaffected members.
MeSH Terms
Adolescent
Adult
Aged
Alkaline Phosphatase/blood
Charcot-Marie-Tooth Disease/enzymology,genetics
Child
Child, Preschool
Female
Genes, Dominant
Genetic Linkage
Humans
Infant
Male
Middle Aged
Muscular Atrophy/genetics
Chemicals
Alkaline Phosphatase
Article Info
Journal
European neurology
Abbr.
Eur Neurol
ISSN
0014-3022
Published
1978-00-00
Pages
336-44
Language
English
Region
Switzerland
NLM ID
0150760
Subset
IM
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