Mapping of Charcot-Marie-Tooth Disease Type 1C to Chromosome 16p Identifies a Novel Locus for Demyelinating Neuropathies

Charcot-Marie-Tooth (CMT) neuropathy represents a genetically heterogeneous group of diseases affecting the peripheral nervous system. We report genetic mapping of the disease to chromosome 16p13.1-p12.3, in two families with autosomal dominant CMT type 1C (CMT1C). Affected individuals in these fami...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Street, Valerie A., Goldy, Jeff D., Golden, Alana S., Tempel, Bruce L, Bird, Thomas D., Chance, Phillip F.
Médium: Artigo
Jazyk:Inglês
Vydáno: The American Society of Human Genetics 2002
Témata:
Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC384893/
https://ncbi.nlm.nih.gov/pubmed/11713717
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky