Hayta, B. Et Al. 2016. A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology.. ESHG , (Barcelona, Spain), 45.

Hayta, B., Puralı, N., Tan, M. E., Erdem Özdamar, S., Talim, B., Korkusuz, P., ... Dinçer, P. R.(2016). A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology. . ESHG (pp.45). Barcelona, Spain

Hayta, BURCU Et Al. "A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology.," ESHG, Barcelona, Spain, 2016

Hayta, BURCU Et Al. "A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology.." ESHG , Barcelona, Spain, pp.45, 2016

Hayta, B. Et Al. (2016) . "A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology.." ESHG , Barcelona, Spain, p.45.

@conferencepaper{conferencepaper, author={BURCU BALCI Et Al. }, title={A novel mutation in the desmin gene DES cause an autosomal recessive form of limb girdle muscular dystrophy type 2R without clear cut desminopathy pathology.}, congress name={ESHG}, city={Barcelona}, country={Spain}, year={2016}, pages={45} }