Add to ORKGRiboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutation
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of diso...
Riboflavin (vitamin B2) plays an important role in cellular growth and function. Riboflavin transpor...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutati...
Background: Brown-Vialetto-Van Laere (BVVL) syndrome is a rare disorder characterised by progressive...
Brown-Vialetto-Van Laere syndrome (BVVLS [MIM 211530]) is a rare neurological disorder characterized...
Investigators at Great Ormond Street Hospital, London, UK, and multiple centers internationally repo...
Brown-Vialetto-Van Laere syndrome is a rare disorder characterized by motor, sensory, and cranial ne...
Brown-Vialetto-Van Laere syndrome (BVVLS) or riboflavin transporter deficiency (OMIM 211530) is a ra...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
We report on three patients (two siblings and one unrelated) presenting in infancy with progressive ...
PubMedID: 26444347Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare and severe neurometabolic dise...
Title Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter ...
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of diso...
Brown-Vialetto-Van Laere syndrome (BVVLS) is a genetic condition caused by a mutation in the C20orf5...
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of diso...
Riboflavin (vitamin B2) plays an important role in cellular growth and function. Riboflavin transpor...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutati...
Background: Brown-Vialetto-Van Laere (BVVL) syndrome is a rare disorder characterised by progressive...
Brown-Vialetto-Van Laere syndrome (BVVLS [MIM 211530]) is a rare neurological disorder characterized...
Investigators at Great Ormond Street Hospital, London, UK, and multiple centers internationally repo...
Brown-Vialetto-Van Laere syndrome is a rare disorder characterized by motor, sensory, and cranial ne...
Brown-Vialetto-Van Laere syndrome (BVVLS) or riboflavin transporter deficiency (OMIM 211530) is a ra...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
We report on three patients (two siblings and one unrelated) presenting in infancy with progressive ...
PubMedID: 26444347Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare and severe neurometabolic dise...
Title Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter ...
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of diso...
Brown-Vialetto-Van Laere syndrome (BVVLS) is a genetic condition caused by a mutation in the C20orf5...
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of diso...
Riboflavin (vitamin B2) plays an important role in cellular growth and function. Riboflavin transpor...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...