Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain

Nature Genetics

Volumn 17, Issue 2, 1997, Pages 146-148

  Gibbons, Richard J ^a   Bachoo, Satvinder ^a   Picketts, David J ^a   Aftimos, Salim ^b   Asenbauer, Bernhard ^c   Bergoffen, Joann ^d   Berry, Susan A ^e   Dahl, Niklas ^f   Fryer, Alan ^g   Keppler, Kim ^h   Kurosawa, Kenji ⁱ   Levin, Michael L ^j   Masuno, Mitsuo ^k   Neri, Giovanni ^l   Pierpont, Mary Ella ^e   Slaney, Sarah F ^m   Higgs, Douglas R ^a  

^a JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^b AUCKLAND CITY HOSPITAL   (New Zealand)

^c UNIVERSITY OF TÜBINGEN   (Germany)

^d KAISER PERMANENTE MEDICAL CENTER   (United States)

^e UNIVERSITY OF MINNESOTA   (United States)

^f UNIVERSITY CHILDREN S HOSPITAL   (Sweden)

^g ALDER HEY CHILDREN S HOSPITAL   (United Kingdom)

^h UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

ⁱ Tokyo Metropolitan Kita Medical Rehabilitation Center for the Handicapped   (Japan)

^j UNIVERSITY OF NEVADA SCHOOL OF MEDICINE   (United States)

^k KANAGAWA CHILDREN'S MEDICAL CENTER   (Japan)

^l CATHOLIC UNIVERSITY   (Italy)

^m UNIVERSITY COLLEGE LONDON   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ATRX PROTEIN, HUMAN; ATRX PROTEIN, MOUSE; DNA BINDING PROTEIN; GLOBIN; HELICASE; NUCLEAR PROTEIN; TRANSCRIPTION FACTOR; ZINC FINGER PROTEIN;

ALPHA THALASSEMIA; AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; GENETICS; HUMAN; LETTER; MENTAL DEFICIENCY; MOLECULAR GENETICS; MOUSE; MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; SEQUENCE HOMOLOGY; SYNDROME;

ALPHA-THALASSEMIA; AMINO ACID SEQUENCE; ANIMALS; CONSERVED SEQUENCE; DNA HELICASES; DNA-BINDING PROTEINS; GLOBINS; HUMANS; MENTAL RETARDATION; MICE; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEAR PROTEINS; PHENOTYPE; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME; TRANSCRIPTION FACTORS; ZINC FINGERS;

EID: 0031255159     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1097-146     Document Type: Letter

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