| 1 | MPTLT3, MPTLT4, CHRNA1, CHRND |
| Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. | |
| Michalk A, Stricker S, Becker J, Rupps R, Pantzar T, Miertus J, Botta G, Naretto VG, Janetzki C, Yaqoob N, Ott CE, Seelow D, Wieczorek D, Fiebig B, Wirth B, Hoopmann M, Walther M, Kšrber F, Blankenburg M, Mundlos S, Heller R, Hoffmann K. | |
| Am J Hum Genet 82(2):464-76. 2008 | |