Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis

Translational Neurodegeneration

Volumn 4, Issue 1, 2015, Pages

  Yamashita, Satoshi ^a   Ando, Yukio ^a  

^a KUMAMOTO UNIVERSITY   (Japan)

Author keywords

Amyotrophic lateral sclerosis (ALS); Familial ALS (FALS); Genotype; Phenotype; Sporadic ALS (SALS)

Indexed keywords

ALSIN; ANGIOGENIN; ATAXIN 2; CHROMATIN MODIFYING PROTEIN 2B; COILED COIL HELIX COILED COIL HELIX DOMAIN CONTAINING 10 PROTEIN; COPPER ZINC SUPEROXIDE DISMUTASE; CYSTEINE PROTEINASE; EPIDERMAL GROWTH FACTOR RECEPTOR 4; FIG4 HOMOLOG PROTEIN; FUSED IN SARCOMA PROTEIN; HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN; HETEROGENEOUS NUCLEAR RIBONUCLEOPROTEIN A1; MATRILYSIN; MATRIN 3; MEMBRANE PROTEIN; OPTINEURIN; PROFILIN; PROFILIN 1; PROTEIN KINASE; RECEPTOR; SENATAXIN; SIGMA NON OPIOID RECEPTOR; SPASTIC PARAPLEGIA 11 PROTEIN; TANK BINDING KINASE 1; TAR DNA BINDING PROTEIN; UBIQUILIN 2; UNCLASSIFIED DRUG; VALOSIN CONTAINING PROTEIN; VESICLE ASSOCIATED MEMBRANE PROTEIN ASSOCIATED PROTEIN B;

AMYOTROPHIC LATERAL SCLEROSIS; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CHROMOSOME 9; DIAGNOSTIC ACCURACY; DISEASE CLASSIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; MOLECULAR GENETICS; MOLECULAR PATHOLOGY; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN ANALYSIS; REVIEW; SEQUENCE ANALYSIS;

EID: 84937810438     PISSN: None     EISSN: 20479158     Source Type: Journal    
DOI: 10.1186/s40035-015-0036-y     Document Type: Review

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