Latest Article Alert from Orphanet Journal of Rare Diseases

The following new article has just been published in Orphanet Journal of Rare Diseases

Letter to the Editor  

Posterior cortical atrophy as a primary clinical phenotype of corticobasal syndrome with a progranulin gene rs5848 TT genotype

Peng G, Liu P, He F, Luo B

Orphanet Journal of Rare Diseases 2016, 11 :13 (6 February 2016)

Abstract | Full Text | PDF