Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codon

Nucleic Acids Research

Volumn 36, Issue 1, 2008, Pages 237-244

  Rederstorff, M ^a,f   Allamand, V ^b,c   Guicheney, P ^b,c   Gartioux, C ^b,c   Richard, P ^b,c,d   Chaigne, D ^e   Krol, A ^a   Lescure, A ^a  

^a INST DE BIOL MOLEC ET CELLULAIRE   (France)

^b INSERM   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^e Clinique Sainte Odile   (France)

^f INNSBRUCK MEDICAL UNIVERSITY   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

SELENOCYSTEINE; SELENOPROTEIN; SELENOPROTEIN N; TRANSFER RNA; UNCLASSIFIED DRUG;

ARTICLE; CODON; CONTROLLED STUDY; FIBROBLAST; GENE EXPRESSION; GENETIC DISORDER; HELA CELL; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; MOLECULAR CLONING; MUSCLE DISEASE; NONSENSE MUTATION; PRIORITY JOURNAL; PROTEIN DEFICIENCY; PROTEIN DEGRADATION; PROTEIN SYNTHESIS; SELENOPROTEIN N DEFICIENCY; SPINAL MUSCULAR ATROPHY;

CODON; CODON, NONSENSE; FIBROBLASTS; HELA CELLS; HUMANS; MUSCLE PROTEINS; MUSCULAR ATROPHY, SPINAL; RNA, TRANSFER, AMINO ACID-SPECIFIC; SELENOCYSTEINE; SELENOPROTEINS; TRANSGENES;

EID: 38349180726     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkm1033     Document Type: Article

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