Title: | Epigenetic hypomethylation in FSHD: It's not what you inherit, it's whether it shows |
Journal : | Neurology, 83, 8 |
Authors: | Lunt PW ; Figlewicz DA |
Material Type: | Article |
Publication Date: | 2014 |
Size: | p 674 |
Languages: | English |
Keywords : | dystrophie musculaire facio-scapulo-humérale de type 2 ; facioscapulohumeral muscular dystrophy ; genetic diagnosis ; genotype-phenotype correlation ; methylation ; parental imprinting |
Abstract: |
Comment on:
Differential DNA methylation of the D4Z4 repeat in patients with FSHD and asymptomatic carriers. Gaillard MC, Roche S, Dion C, Tasmadjian A, Bouget G, Salort-Campana E, Vovan C, Chaix C, Broucqsault N, Morere J, Puppo F, Bartoli M, Levy N, Bernard R, Attarian S, Nguyen K, Magdinier F. Neurology. 2014 Aug 19;83(8):733-42. |
Pubmed / DOI : | DOI : 10.1212/WNL.0000000000000726 / Pubmed : 25031285 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/25031285 |
See also : |