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A new homozygous missense variant in LMOD3 gene causing mil..:
Segarra-Casas, Alba
;
Collet, Roger
;
Gonzalez-Quereda, Lidia
...
Neuromuscular Disorders. 33 (2023) 4 - p. 319-323 , 2023
Link:
https://doi.org/10.1016/j.nmd.2023.02.006
RT Journal T1
A new homozygous missense variant in LMOD3 gene causing mild nemaline myopathy with prominent facial weakness
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.nmd.2023.02.006&Exemplar=1&LAN=DE A1 Segarra-Casas, Alba A1 Collet, Roger A1 Gonzalez-Quereda, Lidia A1 Vesperinas, Ana A1 Caballero-Ávila, Marta A1 Carbayo, Alvaro A1 Díaz-Manera, Jordi A1 Rodriguez, María José A1 Gallardo, Eduard A1 Gallano, Pia A1 Olivé, Montse PB Elsevier BV YR 2023 SN 0960-8966 JF Neuromuscular Disorders VO 33 IS 4 SP 319 OP 323 LK http://dx.doi.org/https://doi.org/10.1016/j.nmd.2023.02.006 DO https://doi.org/10.1016/j.nmd.2023.02.006 SF ELIB - SuUB Bremen
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