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

T Ozcelik, N Akarsu, E Uz, S Caglayan… - Proceedings of the …, 2008 - National Acad Sciences
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …

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

T Ozcelik, A AKARSU, E Uz… - … OF SCIENCES OF …, 2008 - avesis.acibadem.edu.tr
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …

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

T Ozcelik, N Akarsu, E Uz, S Caglayan… - Proceedings of the …, 2008 - europepmc.org
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …

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

T Ozcelik, N Akarsu, E Uz, S Caglayan, S Gulsuner… - PNAS, 2008 - sedivy.net
Results The proband of Family A (12) is a 37-year-old male with habitual quadrupedal gait
(Fig. 1A Upper Left and Fig. 2A, VI: 20). He did not make the transition to bipedality during …

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

T Ozcelik, N Akarsu, E Uz, S Caglayan… - Proceedings of the …, 2008 - hero.epa.gov
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …

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

T Ozcelik, N Akarsu, E Uz, S Caglayan, S Gulsuner… - PNAS, 2008 - researchgate.net
Results The proband of Family A (12) is a 37-year-old male with habitual quadrupedal gait
(Fig. 1A Upper Left and Fig. 2A, VI: 20). He did not make the transition to bipedality during …

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

T Ozcelik, N Akarsu, E Uz, S Caglayan… - Proceedings of the …, 2008 - ui.adsabs.harvard.edu
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …

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

T Ozcelik, N Akarsu, E Uz, S Caglayan, S Gulsuner… - PNAS, 2008 - repository.bilkent.edu.tr
Results The proband of Family A (12) is a 37-year-old male with habitual quadrupedal gait
(Fig. 1A Upper Left and Fig. 2A, VI: 20). He did not make the transition to bipedality during …

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

T Ozcelik, N Akarsu, E Uz… - Proceedings of the …, 2008 - pubmed.ncbi.nlm.nih.gov
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …

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

T Ozcelik, A Akarsu, E Uz, S Caglayan… - … OF SCIENCES OF …, 2008 - avesis.hacettepe.edu.tr
Quadrupedal gait in humans, also known as Unertan syndrome, is a rare phenotype
associated with dysarthric speech, mental retardation, and varying degrees of …