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Identification of mutations in...
Čujuhandieđut
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Doalvun: RefWorks
Doalvun: EndNoteWeb
Doalvun: EndNote
Bissovaš liŋka
Identification of mutations in ATRX by RNase mismatch cleavage.
Bibliográfalaš dieđut
Váldodahkkit:
Gibbons, R
,
Bachoo, S
,
Picketts, D
,
Higgs, DR
Materiálatiipa:
Journal article
Almmustuhtton:
1997
Oažžasuvvandieđut
Govvádus
Geahča maid
Bargiidšearbma
Geahča maid
ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
Dahkki: Picketts, D, et al.
Almmustuhtton: (1996)
Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
Dahkki: Picketts, D, et al.
Almmustuhtton: (1998)
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
Dahkki: Gibbons, R, et al.
Almmustuhtton: (1997)
Disruption of ATRX in mouse by conditional knockout.
Dahkki: Gibbons, R, et al.
Almmustuhtton: (2002)
Detection of mutations by RNase cleavage.
Dahkki: Watkins, H, et al.
Almmustuhtton: (2001)