Carriers month spinal muscular atrophies of childhood. 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 Motor Neuron Disease Spinal Cord Diseases Neuromuscular Junction Diseases Optic Atrophy Arthrogryposis Contracture Neuromuscular Diseases Nerve Degeneration Charcot-Marie-Tooth Disease Fasciculation Vocal Cord Paralysis Muscle Weakness Respiratory Paralysis Multiple System Atrophy Muscular Dystrophies Amyotrophic Lateral Sclerosis Spinal Cord Neoplasms Hereditary Sensory and Motor Neuropathy Spinal Diseases Spinal Cord Compression Spinal Neoplasms Bulbar Palsy, Progressive

Chemicals and Drugs19

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 Carrier Proteins Heterogeneous-Nuclear Ribonucleoprotein Group A-B RNA, Messenger Oligonucleotides, Antisense Drug Carriers

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

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

Psychiatry and Psychology1

Phenomena and Processes19

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

Disciplines and Occupations2

Genetic Counseling Chemistry, Analytic

Information Science2

Molecular Sequence Data Base Sequence

Named Groups1

Infant, Newborn

Health Care3

Genetic Counseling Genetic Testing Carrier State

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

Muscular Atrophy, Spinal Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein SMN Complex Proteins 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 Exons Spinal Cord Injuries Coiled Bodies snRNP Core Proteins Heterozygote Detection Disease Models, Animal Motor Neuron Disease Spinal Cord Diseases Pedigree Phenotype Glycine-tRNA Ligase Gene Deletion Homozygote Neuromuscular Junction Diseases RNA Splicing Mice, Transgenic Muscle, Skeletal Mutation Optic Atrophy Arthrogryposis Neuromuscular Junction Gene Dosage Axons Contracture Genes, Recessive Electromyography Prenatal Diagnosis Genetic Counseling Heterozygote Neuromuscular Diseases Nerve Degeneration Chemistry, Analytic Genetic Linkage Charcot-Marie-Tooth Disease Genes, Dominant Genetic Testing Fasciculation Vocal Cord Paralysis Injections, Spinal Spinal Nerve Roots Carrier State Spliceosomes Alternative Splicing Muscle Weakness Molecular Sequence Data Respiratory Paralysis Neural Conduction Valproic Acid Spinal Nerves Infant, Newborn Base Sequence Multiple System Atrophy Muscular Dystrophies Aclarubicin Anesthesia, Spinal Fibroblasts Mutation, Missense Motor Activity Amyotrophic Lateral Sclerosis Receptors, Androgen Spinal Cord Neoplasms Carrier Proteins Polymerase Chain Reaction Genotype Spinal Canal Hereditary Sensory and Motor Neuropathy Genetic Therapy HeLa Cells Heterogeneous-Nuclear Ribonucleoprotein Group A-B Magnetic Resonance Imaging Spinal Diseases Spinal Cord Compression DNA Mutational Analysis Muscle Strength Dynamometer RNA, Messenger Alleles Spinal Neoplasms Chromosome Mapping Mice, Knockout Muscles Oligonucleotides, Antisense

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