Pelin K.,1997
Pelin K., Ridanpaa M., Donner K., Wilton S., Krishnarajab J., Laing N., Kolmerer B., Millevoi S., Labeit S., de la Chapelle A., Wallgren-Pettersson C. Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy. - Eur.J.Hum.Genet., 1997, v. 5, p. 229-234.
