Human desmin gene: cDNA sequence, regional localization and exclusion of the locus in a familial desmin-related myopathy

Human Genetics

Volumn 98, Issue 4, 1996, Pages 422-429

  Vicart, Patrick ^a   Dupret, Jean Marie ^a,c   Hazan, Jamilé ^b   Li, Zhenlin ^a   Gyapay, Gabor ^b   Krishnamoorthy, Rajagopal ^c   Weissenbach, Jean ^b   Fardeau, Michel ^d   Paulin, Denise ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b GÉNÉTHON   (France)

^c HÔPITAL ROBERT DEBRÉ   (France)

^d INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; DESMIN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME; CHROMOSOME 2Q; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; EXON; FEMALE; GENE FUNCTION; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; INTERMEDIATE FILAMENT; MALE; MARKER GENE; MOLECULAR CLONING; MYOPATHY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SARCOPLASM;

MUS MUSCULUS;

EID: 0029814021     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050233     Document Type: Article

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