Citations for
1TIA1, WDM
Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1.
Hackman P, Sarparanta J, Lehtinen S, Vihola A, Evilä A, Jonson PH, Luque H, Kere J, Screen M, Chinnery PF, Åhlberg G, Edström L, Udd B.
Ann Neurol. Apr;73(4):500-9. doi: 10.1002/ana.23831. Epub 2013 Feb 11. 2013
2TIA1, WDM
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus.
von Tell D, Bruder CE, Anderson LV, Anvret M, Ahlberg G.
Neurogenetics. Aug;4(4):173-7. doi: 10.1007/s10048-003-0154-z. Epub 2003 Jun 27. 2003
3WDM
Genetic linkage of Welander distal myopathy to chromosome 2p13.
Ahlberg G, von Tell D, Borg K, Edstrom L, Anvret M.
Ann Neurol 46(3):399-404. 1999