Neurology · 2006 · 104 citations · 32 references
Charcot-Marie-Tooth type 4C (CMT4C) is less severe than other autosomal recessive (AR) CMT. Intrafamilial variability is important, making phenotype-genotype correlations difficult, but spine deformities are clearly a hallmark of CMT4C. In the presence of scoliosis, a neurologic examination is recommended. Giant axons on biopsies are also suggestive of CMT4C. For genetic analysis, the R954X mutation should be looked for before systematic sequencing of exon 11.
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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.
G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · PubMed · 1985 · 1.2K citations
Genetic and clinical aspects of Charcot‐Marie‐Tooth's disease
H. Skre · Clinical Genetics · 1974 · 897 citations
Avoiding Recomputation in Linkage Analysis
Alejandro A. Sch auml ffer, Sandeep Gupta, Kartheek Medhavi Penagamuri Shriram et al. · Human Heredity · 1994 · 673 citations