The Ig-like structure of the C-terminal domain of lamin A/C, mutated in muscular dystrophies, cardiomyopathy, and partial lipodystrophy

Structure

Volumn 10, Issue 6, 2002, Pages 811-823

  Krimm, Isabelle ^a   Östlund, Cecilia ^b   Gilquin, Bernard ^a   Couprie, Joël ^a   Hossenlopp, Paul ^c   Mornon, Jean Paul ^c   Bonne, Gisèle ^d   Courvalin, Jean Claude ^e   Worman, Howard J ^b   Zinn Justin, Sophie ^a  

^a CEA SACLAY   (France)

^b The New York Presbyterian Hospital   (United States)

^c UNIVERSITÉ PIERRE ET MARIE CURIE   (France)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e INSTITUT JACQUES MONOD   (France)

Author keywords

Dystrophy; Ig fold; Lamin; Laminopathies; NMR; Nuclear lamina

Indexed keywords

IMMUNOGLOBULIN; LAMIN A; LAMIN C; MUTANT PROTEIN;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CARDIOMYOPATHY; CIRCULAR DICHROISM; DUNNIGAN LIPODYSTROPHY; EMERY DREIFUSS MUSCULAR DYSTROPHY; GENETIC DISORDER; LIPODYSTROPHY; MISSENSE MUTATION; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FOLDING; PROTEIN STRUCTURE; STRUCTURE ANALYSIS; THERMOSTABILITY;

EID: 18444382032     PISSN: 09692126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0969-2126(02)00777-3     Document Type: Article

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