New phenotype of DCTN1‐related spectrum: early‐onset dHMN plus congenital foot deformity
Cited by 9
Related Papers
Frequent Mutation of <i>BAP1</i> in Metastasizing Uveal Melanomas
|Science|2010|1.5k
PSORS2 Is Due to Mutations in CARD14
|The American Journal of Human Genetics|2012|414
Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
|The American Journal of Human Genetics|2012|357