Nuclear matrix proteins and hereditary diseases

Genetika

Volumn 41, Issue 3, 2005, Pages 293-298

  Sjakste, N ^a   Sjakste, T ^a  

^a UNIVERSITY OF LATVIA   (Latvia)

Author keywords

[No Author keywords available]

Indexed keywords

EMERIN; ENZYME; LAMIN A; LAMIN B; LAMIN C; NUCLEAR MATRIX PROTEIN; POLYGLUTAMIC ACID; PROTEIN DERIVATIVE;

AUTOSOMAL RECESSIVE DISORDER; AXONAL INJURY; BONE DYSPLASIA; CANCER; CELL DIFFERENTIATION; CELL GROWTH; COCKAYNE SYNDROME; CONGESTIVE CARDIOMYOPATHY; DENTATORUBROPALLIDOLUYSIAN ATROPHY; DISEASE CLASSIFICATION; DISORDERS OF CARBOHYDRATE METABOLISM; DNA REPAIR; DOWN SYNDROME; EMERY DREIFUSS MUSCULAR DYSTROPHY; FAMILIAL DISEASE; FANCONI ANEMIA; GENE EXPRESSION; GENE FUNCTION; GENE MUTATION; GENE STRUCTURE; GENETIC DISORDER; GENETIC REGULATION; HEART MUSCLE CONDUCTION DISTURBANCE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUNTINGTON CHOREA; LEUKOCYTE DISORDER; LIMB GIRDLE MUSCULAR DYSTROPHY; LIPODYSTROPHY; MYOTONIC DYSTROPHY; NEUROPATHY; NUCLEAR LAMINA; PREMATURE AGING; PROGERIA; PROTEIN SYNTHESIS; RECEPTOR GENE; REVIEW; WERNER SYNDROME; ANIMAL; GENE EXPRESSION REGULATION; GENETICS;

ANIMALS; DNA REPAIR; GENE EXPRESSION REGULATION; GENETIC DISEASES, INBORN; HUMANS; NUCLEAR MATRIX-ASSOCIATED PROTEINS;

EID: 20344369553     PISSN: 00166758     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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