kw.\*:("RYRI mutations")
Results 1 to 1 of 1
Selection :
Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesiaROMERO, Norma Beatriz; MONNIER, Nicole; VIOLLET, Louis et al.Brain. 2003, Vol 126, pp 2341-2349, issn 0006-8950, 9 p., 11Article