Title: | Autosomal-recessive Charcot-Marie-Tooth diseases |
Journal : | Journal of neuropathology and experimental neurology, 64, 5 |
Authors: | Vallat JM ; Tazir M ; Magdelaine C ; Sturtz F ; Grid D |
Material Type: | Article |
Publication Date: | 05/2005 |
Size: | p. 363-370 |
Languages: | English |
Keywords : | Algeria ; axonal forms of CMT ; biomedical research ; CMT2 autosomal recessive form ; CMT4A ; CMT4B1 ; CMT4B2 ; CMT4C ; CMT4D ; CMT4E ; CMT4G ; CMT4H ; consanguinity ; diseases classifications ; EGR2 protein related CMT4E ; electron microscopy ; GDAP1 gene ; genetic linkage ; genetic mutations ; genotype-phenotype correlation ; histopathology ; lamins ; MTMR2 gene ; nerve biopsies ; periaxin ; spinal muscular atrophy with respiratory distress type 1 |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15892292&query_hl=19 |
Pubmed / DOI : | Pubmed : 15892292 |