Seminars in Pediatric Neurology
Volume 15, Issue 4 , Page 159 , December 2008

Editorial Comment

References 

  1. Tischfield MA, Bosley TM, Salih MA, et al. Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development. Nat Genet. 2005;37:1035–1037
  2. Rodier PM, Ingram JL, Tisdale B, et al. Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei. Comp Neurol. 1996;370:247–261
  3. Bosley TM, Alorainy IA, Salih MA, et al. The clinical spectrum of homozygous HOXA1 mutations. Am J Med Genet A. 2008;146A:1235–1240

PII: S1071-9091(08)00072-7

doi: 10.1016/j.spen.2008.09.005

Seminars in Pediatric Neurology
Volume 15, Issue 4 , Page 159 , December 2008

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