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

Gibbons RJ.; Bachoo S.; Picketts DJ.; Aftimos S.; Asenbauer B.; Bergoffen J.; Berry SA.; Dahl N.; Fryer A.; Keppler K.; Kurosawa K.; Levin ML.; Masuno M.; Neri G.; Pierpont ME.; Slaney SF.; Higgs DR.

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

Gibbons RJ., Bachoo S., Picketts DJ., Aftimos S., Asenbauer B., Bergoffen J., Berry SA., Dahl N., Fryer A., Keppler K., Kurosawa K., Levin ML., Masuno M., Neri G., Pierpont ME., Slaney SF., Higgs DR.

Original publication

DOI

10.1038/ng1097-146

Type

Journal article

Journal

Nat Genet

Publication Date

10/1997

Volume

Pages

146 - 148

Keywords

Amino Acid Sequence, Animals, Conserved Sequence, DNA Helicases, DNA-Binding Proteins, Globins, Humans, Intellectual Disability, Mice, Molecular Sequence Data, Mutation, Nuclear Proteins, Phenotype, Sequence Homology, Amino Acid, Syndrome, Transcription Factors, X-linked Nuclear Protein, Zinc Fingers, alpha-Thalassemia