Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).
Dick KJ, Eckhardt M, Paisán-Ruiz C, Alshehhi AA, Proukakis C, Sibtain NA, Maier H, Sharifi R, Patton MA, Bashir W, Koul R, Raeburn S, Gieselmann V, Houlden H, Crosby AH.
Dick KJ, et al. Among authors: sibtain na.
Hum Mutat. 2010 Apr;31(4):E1251-60. doi: 10.1002/humu.21205.
Hum Mutat. 2010.
PMID: 20104589