Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome

Nature

Volumn 384, Issue 6609, 1996, Pages 567-570

  Trivier, Elisabeth ^a   De Cesare, Dario ^a   Jacquot, Sylvie ^a   Pannetier, Solange ^a   Zackai, Elaine ^b   Young, Ian ^c   Mandel, Jean Louis ^a   Sassone Corsi, Paolo ^a   Hanauer, André ^a  

^a CNRS   (France)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c NOTTINGHAM CITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DNA; GROWTH FACTOR; PROTEIN; PROTEIN KINASE;

ARTICLE; CLINICAL ARTICLE; COFFIN LOWRY SYNDROME; FEMALE; GENE; GENE EXPRESSION; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; HUMAN; IMMUNOPRECIPITATION; MALE; MISSENSE MUTATION; PHOSPHORYLATION; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM; SOUTHERN BLOTTING; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; AMINO ACID SEQUENCE; BASE SEQUENCE; CELL LINE; CHROMOSOME MAPPING; FEMALE; FRAMESHIFT MUTATION; HUMANS; MALE; MENTAL RETARDATION; MOLECULAR SEQUENCE DATA; MUTATION; PHOSPHORYLATION; POINT MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEIN-SERINE-THREONINE KINASES; RIBOSOMAL PROTEIN S6; RIBOSOMAL PROTEIN S6 KINASES; RIBOSOMAL PROTEINS; SEX CHROMOSOME ABERRATIONS; SIGNAL TRANSDUCTION; X CHROMOSOME;

EID: 0029832136     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/384567a0     Document Type: Article

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