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Bi-allelic mutations in MYL1 cause a severe congenital myop..:
Ravenscroft, Gianina
;
Zaharieva, Irina
;
Bortolotti, Carlo A
...
Human Molecular Genetics. , 2018
Link:
https://doi.org/10.1093/hmg/ddy320
RT Journal T1
Bi-allelic mutations in MYL1 cause a severe congenital myopathy
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_hmg_ddy320&Exemplar=1&LAN=DE A1 Ravenscroft, Gianina A1 Zaharieva, Irina A1 Bortolotti, Carlo A A1 Lambrughi, Matteo A1 Pignataro, Marcello A1 Borsari, Marco A1 Sewry, Caroline A A1 Phadke, Rahul A1 Haliloglu, Goknur A1 Ong, Royston A1 Goullée, Hayley A1 Whyte, Tamieka A1 Manzur, Adnan A1 Talim, Beril A1 Kaya, Ulkuhan A1 Osborn, Daniel PS A1 Forrest, Alistair A1 Laing, Nigel G A1 Muntoni, Francesco A1 UK10K Consortium PB Oxford University Press (OUP) YR 2018 SN 0964-6906 SN 1460-2083 JF Human Molecular Genetics LK http://dx.doi.org/https://doi.org/10.1093/hmg/ddy320 DO https://doi.org/10.1093/hmg/ddy320 SF ELIB - SuUB Bremen
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