{"symbol":"FRA12A","synonyms":[],"name":"fragile site, folic acid type, rare, fra(12)(q13.1)","description":"FRA12A is a folate-sensitive chromosomal fragile site prone to breakage. No consistent phenotype has been observed with FRA12A, and it can be inherited without phenotypic effect (Berg et al., 2000 [PubMed 10955484]). However, mental retardation with or without other anomalies has been described in patients with over 40% of cells expressing FRA12A (Winnepenninckx et al., 2007).[supplied by OMIM, Mar 2008]","ncbiEntrezGeneId":2448,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/2448","proteins":[],"hgncRootFamilies":[]}