Infantile onset spinal muscular atrophy. Medical search. Frequent questions

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Anatomy16

Spinal Cord Motor Neurons Anterior Horn Cells Chromosomes, Human, Pair 5 Coiled Bodies Muscle, Skeletal Neuromuscular Junction Axons Spinal Nerve Roots Spliceosomes Spinal Nerves Fibroblasts Spinal Canal HeLa Cells Muscles Growth Cones

Organisms2

Mice, Transgenic Mice, Knockout

Diseases30

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Muscular Atrophy Atrophy Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Disease Models, Animal Spinal Cord Diseases Motor Neuron Disease Neuromuscular Junction Diseases Optic Atrophy Arthrogryposis Contracture Nerve Degeneration Neuromuscular Diseases Charcot-Marie-Tooth Disease Fasciculation Vocal Cord Paralysis Muscle Weakness Respiratory Paralysis Multiple System Atrophy Amyotrophic Lateral Sclerosis Muscular Dystrophies Spinal Cord Neoplasms Hereditary Sensory and Motor Neuropathy Spinal Cord Compression Spinal Diseases Spinal Neoplasms Bulbar Palsy, Progressive

Chemicals and Drugs17

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Neuronal Apoptosis-Inhibitory Protein Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 snRNP Core Proteins Glycine-tRNA Ligase Valproic Acid Aclarubicin Receptors, Androgen Heterogeneous-Nuclear Ribonucleoprotein Group A-B RNA, Messenger Oligonucleotides, Antisense

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Disease Models, Animal Pedigree Heterozygote Detection Electromyography Prenatal Diagnosis Injections, Spinal Anesthesia, Spinal Genetic Testing Genetic Therapy Muscle Strength Dynamometer Magnetic Resonance Imaging Polymerase Chain Reaction Chromosome Mapping

Psychiatry and Psychology1

Phenomena and Processes17

Chromosomes, Human, Pair 5 Exons Gene Deletion Phenotype RNA Splicing Homozygote Gene Dosage Mutation Genes, Recessive Genes, Dominant Genetic Linkage Alternative Splicing Neural Conduction Motor Activity Base Sequence Mutation, Missense Heterozygote

Disciplines and Occupations2

Chemistry, Analytic Genetic Counseling

Information Science2

Molecular Sequence Data Base Sequence

Health Care3

Age of Onset Genetic Counseling Genetic Testing

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Health Care

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein SMN Complex Proteins Age of Onset Survival of Motor Neuron 2 Protein Muscular Atrophy Atrophy Neuronal Apoptosis-Inhibitory Protein Spinal Cord Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Motor Neurons Anterior Horn Cells Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Muscular Disorders, Atrophic Chromosomes, Human, Pair 5 Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Exons Coiled Bodies snRNP Core Proteins Disease Models, Animal Spinal Cord Diseases Motor Neuron Disease Pedigree Heterozygote Detection Glycine-tRNA Ligase Gene Deletion Neuromuscular Junction Diseases Mice, Transgenic Phenotype RNA Splicing Homozygote Muscle, Skeletal Optic Atrophy Arthrogryposis Neuromuscular Junction Gene Dosage Axons Electromyography Contracture Mutation Nerve Degeneration Neuromuscular Diseases Chemistry, Analytic Charcot-Marie-Tooth Disease Genes, Recessive Fasciculation Genes, Dominant Prenatal Diagnosis Vocal Cord Paralysis Genetic Linkage Spinal Nerve Roots Injections, Spinal Genetic Counseling Spliceosomes Muscle Weakness Alternative Splicing Respiratory Paralysis Neural Conduction Spinal Nerves Valproic Acid Multiple System Atrophy Anesthesia, Spinal Genetic Testing Amyotrophic Lateral Sclerosis Aclarubicin Fibroblasts Molecular Sequence Data Receptors, Androgen Muscular Dystrophies Motor Activity Base Sequence Spinal Cord Neoplasms Mutation, Missense Spinal Canal Hereditary Sensory and Motor Neuropathy Genetic Therapy Heterogeneous-Nuclear Ribonucleoprotein Group A-B HeLa Cells Spinal Cord Compression Spinal Diseases Muscle Strength Dynamometer Magnetic Resonance Imaging RNA, Messenger Spinal Neoplasms Polymerase Chain Reaction Heterozygote Mice, Knockout Muscles Chromosome Mapping Growth Cones Oligonucleotides, Antisense Bulbar Palsy, Progressive

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