Decoding common and complex genotypes of facioscapulohumeral muscular dystrophy using methylation profiling and long-read sequencing.
Overview & Synopsis
Open access biomedical research article published in Brain Commun.
Indexed from repository: PubMed Central
(
pmc.ncbi.nlm.nih.gov)
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Document Information
| Document Title | Decoding common and complex genotypes of facioscapulohumeral muscular dystrophy using methylation profiling and long-read sequencing. |
|---|---|
| Author / Organization | Scharf F, Lucas MC, Gehling S, Kleefeld F, Schönrock V, Benet-Pagès A, Rausch HW, Schirmer L, Schäfer J, Saak A, Porrmann J, Hütter S, Emde C, Boblest A, Neuhoff S, Hagenacker T, Burkart S, Mingers S, Berking AC, Olfe L, Hendrich C, Schröck K, Sauer E, Mossakowski AA, Sendelbach K, Koehler U, Becker K, Bartolomaeus T, Hallermayr A, Klink B, Neuhann T, Walter MC, Schoser B, Abicht A, Erdmann H |
| Subject & Discipline | Brain Commun |
| Categories | Medicine & Health |
| Publication Year | 2026 |
| License / Rights | Open Access / Creative Commons |
| Resource Verification | Listed PDF (Verification Pending) |
| Original Host Website |
PubMed Central
(pmc.ncbi.nlm.nih.gov)
|
| File Format | application/pdf (Portable Document Format) |
| Language | EN |
| Catalog ID | DOC-80271 |
| Original Source Link | Visit Source Page on pmc.ncbi.nlm.nih.gov » |