Cerebellar ataxia, mental retardation and dysequilibrium syndrome 1 (CAMRQ1) caused by an unusual constellation of VLDLR mutation

Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE)

(2010) Lihadh Al-Gazali et al.   HUMAN MUTATION

Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy

(2010) Luis E. Kolb et al.   NEUROGENETICS

Role for Reelin in stabilizing cortical architecture

(2010) Michael Frotscher   TRENDS IN NEUROSCIENCES

Mutations in VLDLR as a Cause for Autosomal Recessive Cerebellar Ataxia With Mental Retardation (Dysequilibrium Syndrome)

(2009) Kym M. Boycott et al.   JOURNAL OF CHILD NEUROLOGY

Cerebellar hypoplasia, with quadrupedal locomotion, caused by mutations in the very low-density lipoprotein receptor gene

(2008) S Türkmen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans

(2008) T. Ozcelik et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA