Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion

Eitemau Tebyg

• Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans
  gan: Ozcelik, Tayfun, et al.
  Cyhoeddwyd: (2008)
• Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
  gan: Emre Onat, Onur, et al.
  Cyhoeddwyd: (2013)
• Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred
  gan: Gulsuner, Suleyman, et al.
  Cyhoeddwyd: (2011)
• Human quadrupedalism is not an epiphenomenon caused by neurodevelopmental malformation and ataxia
  gan: Karaca, Sibel, et al.
  Cyhoeddwyd: (2012)
• Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor
  gan: Unal Gulsuner, Hilal, et al.
  Cyhoeddwyd: (2015)