Fingerprint
Dive into the research topics of 'Whole-exome sequencing identifies mutated C12orf57 in recessive corpus callosum hypoplasia'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Whole-exome sequencing identifies mutated C12orf57 in recessive corpus callosum hypoplasia
Naiara Akizu, Nuri M. Shembesh, Tawfeg Ben-Omran, Laila Bastaki, Asma Al-Tawari, Maha S. Zaki, Roshan Koul, Emily Spencer, Rasim Ozgur Rosti, Eric Scott, Elizabeth Nickerson, Stacey Gabriel, Gilberto Da Gente, Jiang Li, Matthew A. Deardorff, Laura K. Conlin, Margaret A. Horton, Elaine H. Zackai, Elliott H. Sherr*, Joseph G. Gleeson
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
24
Citations
(Scopus)