- Sherr, Elliott;
- Marsh, APL;
- Lukic, V;
- Pope, K;
- Bromhead, C;
- Tankard, R;
- Ryan, MM;
- Yiu, EM;
- Sim, JCH;
- Delatycki, MB;
- Amor, DJ
To determine the molecular basis of a severe neurologic disorder in a large consanguineous family with complete agenesis of the corpus callosum (ACC), pontocerebellar hypoplasia (PCH), and peripheral axonal neuropathy.Assessment included clinical evaluatio
