1.
Ann N Y Acad Sci
; 883(1): 65-68, 1999 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29086969
RESUMO
A novel form of autosomal recessive distal hereditary motor neuronopathy (distal HMN) is reported. The presence of pyramidal signs within the early stages of the disease with persistence of knee hyperreflexia form distinctive clinical features. We have mapped the HMN-J gene to chromosome 9p21.1-p12, within an estimated interval of 1.2-Mb.