Identification and characterization of a mouse homologue of the Spinal Muscular Atrophy-determining gene, survival motor neuron

Keyphrases

• Spinal muscular Atrophy 100%
• Survival Motor Neuron 100%
• Severe Disease 28%
• Spinal Cord 14%
• Deleterious mutations 14%
• In Situ Hybridization 14%
• Cerebellum 14%
• Motor Impairment 14%
• Hippocampus 14%
• Expression Level 14%
• Spinal Motor Neurons 14%
• Alternative Splicing 14%
• Autosomal Recessive 14%
• Age of Onset 14%
• Severe Phenotype 14%
• Muscle Weakness 14%
• Quadriplegia 14%
• Amino Acid Content 14%
• Nervous System 14%
• Chromatolysis 14%
• Homozygous Deletion 14%
• Deletion mutation 14%
• Neuronal Apoptosis Inhibitory Protein 14%
• TFIIH 14%
• Human Survival 14%
• Form Type 14%
• Respiratory Paralysis 14%
• Werdnig-Hoffmann Disease 14%

Neuroscience

• Spinal Muscular Atrophy 100%
• Hippocampus 25%
• Quadriplegia 25%
• Nervous System 25%
• Cerebellum 25%
• Amino Acid 25%
• Autosomal Recessive Disorder 25%
• Neuronal Apoptosis Inhibitory Protein 25%
• Transcription Factor IIH 25%
• Stereotypic Movement Disorder 25%
• In Situ Hybridization 25%
• Messenger RNA 25%