Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability

Journal: Am J Hum Genet

Volume: 

Issue: 

Year of Publication: 2014

Affiliated Institutions: 

Statistics

Citations :  2
Authors :  0

Identifiers

Doi : 10.1016/j.ajhg.2014.10.016
SSN : 

Study Population

Male,Female

Mesh Terms

Other Terms

Study Design

Study Approach

Country of Study

Egypt

Publication Country