Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenital (Becker disease) carrying a new mutation in the CLCN1 gene

F, Morales; P, Cuenca; G, Del Valle; M, Vásquez; R, Brian; M., Sittenfeld

Year:

2008

Type of Publication:

Article

Journal:

Rev Biol Trop

Volume:

56

Number:

1

Pages:

001-011

DOI:

https://doi.org/10.15517/rbt.v56i1.5505