| 1 | KFS4, MYO18B |
| A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B. | |
| Alazami AM, Kentab AY, Faqeih E, Mohamed JY, Alkhalidi H, Hijazi H, Alkuraya FS. | |
| J Med Genet 52(6):400-4. doi: 10.1136/jmedgenet-2014-102964. Epub 2015 Mar 6. 2015 | |