Linkage between the loci for autosomal dominant neuronal Charcot-Marie-Tooth neuropathy (CMT1) and serum amyloid P component (APCS) on human chromosome 1

Cytogenet Cell Genet. 1988;47(3):175-6. doi: 10.1159/000132541.

Authors

V Ionasescu¹, T Burns, C Searby, R Ionasescu, A S Whitehead

Affiliation

¹ Department of Pediatrics, University of Iowa Hospitals, Iowa City 52242.

PMID: 3163970
DOI: 10.1159/000132541

No abstract available

MeSH terms

Charcot-Marie-Tooth Disease / blood
Charcot-Marie-Tooth Disease / genetics*
Chromosome Mapping
Chromosomes, Human, Pair 1*
Genetic Linkage*
Genetic Markers
Humans
Muscular Atrophy, Spinal / genetics*
Serum Amyloid P-Component / blood
Serum Amyloid P-Component / genetics*

Substances

Genetic Markers
Serum Amyloid P-Component