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Volumn 29, Issue 1, 2010, Pages 1-20
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Mendelian bases of myopathies, cardiomyopathies, and neuromyopathies
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Author keywords
[No Author keywords available]
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Indexed keywords
ABC TRANSPORTER;
ACETYLCHOLINESTERASE;
ACTIVIN RECEPTOR LIKE KINASE 1;
ACYL COENZYME A DEHYDROGENASE;
ALPHA ACTIN;
ALPHA CRYSTALLIN;
ANDROGEN RECEPTOR;
BCL2 RELATED PROTEIN A1;
BUNGAROTOXIN RECEPTOR;
CALPAIN;
CAVEOLIN;
CHOLINERGIC RECEPTOR;
COFILIN 2;
COLLAGEN TYPE 6;
CONNEXIN 40;
CONTACTIN;
CYSTEINE;
DESMIN;
DESMOCOLLIN;
DESMOGLEIN 2;
DESMOPLAKIN;
DOCKING PROTEIN;
DYNACTIN;
DYNAMIN II;
GLUCAN 1,4 ALPHA GLUCOSIDASE;
GLYCINE;
GLYCINE RICH PROTEIN;
MESSENGER RNA;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
VOLTAGE GATED CALCIUM CHANNEL;
ACYL COENZYME A DEHYDROGENASE VERY LONG CHAIN DEFICIENCY;
AMYOTROPHIC LATERAL SCLEROSIS;
ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS;
ANDROGEN INSENSITIVITY SYNDROME;
ANTERIOR HORN CELL DISEASE;
ARTHROGRYPOSIS;
ATAXIA;
AUTOSOMAL DOMINANT DISORDER;
BREAST CANCER;
BRUGADA SYNDROME;
CARDIOMYOPATHY;
CARDIOVALVULAR DYSPLASIA;
CARMITINE PALMITOYLTRANSFERASE DEFICIENCY;
CARNEY COMPLEX;
CHANARIN DORFAM SYNDROME;
CHROMOSOME 10;
CHROMOSOME SIZE;
CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA;
CONGENITAL CATARACT;
CONGENITAL FIBROSIS OF THE EXTRAOCULAR MUSCLE;
CONGENITAL GENERALIZED LIPODYSTROPHY;
CONGENITAL HEART DISEASE;
CONGENITAL MYASTHENIC SYNDROME;
CORPUS CALLOSUM AGENESIS;
DNA SEQUENCE;
DYSAUTONOMIA;
EMERY DREIFUSS MUSCULAR DYSTROPHY;
ENDPLATE ACETYCHOLINESTERASE DEFICIENCY;
EPIDERMOLYSIS BULLOSA SIMPLEX;
EPISODIC ATAXIA;
EXON;
FABRY DISEASE;
FACE DYSMORPHIA;
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY;
FAMILIAL PARTIAL LIPODYSTROPHY;
FIBROUS DYSPLASIA;
FRONTOMETAPHYSEAL DYSPLASIA;
FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY;
GENETIC DATABASE;
GENETIC DISORDER;
GENETIC VARIABILITY;
GENOMICS;
GLYCOGEN STORAGE DISEASE;
HEARING IMPAIRMENT;
HEART ARRHYTHMIA;
HEART RIGHT VENTRICLE DYSPLASIA;
HEART VENTRICLE TACHYCARDIA;
HEREDITARY MOTOR SENSORY NEUROPATHY;
HUMAN;
HYPOKALEMIC PERIODIC PARALYSIS;
KARYOTYPE;
KENNEDY DISEASE;
LEUKODYSTROPHY;
LIMB GIRDLE MUSCULAR DYSTROPHY;
LONG QT SYNDROME;
MALIGNANT HYPERTHERMIA;
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME;
MOLECULAR GENETICS;
MUSCLE EYE BRAIN DISEASE;
MYOCLONUS DYSTONIA;
MYOPATHY;
MYOSIN STORAGE MYOPATHY;
MYXOMATOUS VALVULAR DYSTROPHY;
NATURAL LIPID STORAGE DISEASE;
NEMALINE MYOPATHY;
NEUROMUSCULAR DISEASE;
NUCLEOTIDE SEQUENCE;
OCULOPHARYNGEAL MUSCULAR DYSTROPHY;
OPEN READING FRAME;
OSSIFYING MYOSITIS;
PERIVENTRICULAR HETEROTOPIA;
PRIMARY LATERAL SCLEROSIS;
PROSTATE CANCER;
REIFENSTEIN SYNDROME;
REVIEW;
SENSORY ATAXIC NEUROPATHY DYSARTHRIA AND OPHTHALMOPARESIS;
SICK SINUS SYNDROME;
SINGLE NUCLEOTIDE POLYMORPHISM;
SJOEGREN LARSSON SYNDROME;
SPASTIC PARAPLEGIA;
SPINOCEREBELLAR DEGENERATION;
TRISMUS;
TRISMUS PSEUDOCAMPTODACTYLY SYNDROME;
UNINDEXED SEQUENCE;
WALKER WARBURG SYNDROME;
X CHROMOSOME LINKED DISORDER;
CARDIOMYOPATHIES;
DNA MUTATIONAL ANALYSIS;
GENETIC VARIATION;
GENOME, HUMAN;
HUMANS;
MUSCULAR DISEASES;
NEUROMUSCULAR DISEASES;
POLYMORPHISM, SINGLE NUCLEOTIDE;
POLYNEUROPATHIES;
SEQUENCE ANALYSIS, DNA;
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EID: 77956273817
PISSN: 11282460
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (5)
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References (0)
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