New allele of probe D17S61 present in the Charcot‐Marie‐Tooth 1A duplication
- 1 November 1994
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 46 (5) , 380-381
- https://doi.org/10.1111/j.1399-0004.1994.tb04184.x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Charcot–Marie–Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unitNature Genetics, 1992
- Peripheral myelin protein–22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot–Marie–Tooth 1ANature Genetics, 1992
- The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplicationNature Genetics, 1992
- The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1ANature Genetics, 1992
- The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1ANature Genetics, 1992
- DNA duplication associated with Charcot-Marie-Tooth disease type 1ACell, 1991
- Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)Neuromuscular Disorders, 1991