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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
| File Format | PDF (Portable Document Format) |
|---|---|
| Publication Year | 2026 |
| Source Host |
PubMed Central
(pmc.ncbi.nlm.nih.gov)
|
| License / Terms | Open Access / Creative Commons |
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