Gene: [0Xq2/PGS] Pettigrew syndrome; mental retardation, X-linked, syndromic 5 (basal ganglia disease/seizures); [MRXS5 ]

KEY

 neu, devd

CLA

 unknown, basic

LOC

 0X q25-27

MIM

 MIM: 304340

SYN

 MRXS5