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Identification of mutations in...
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Identification of mutations in ATRX by RNase mismatch cleavage.
Bibliografske podrobnosti
Main Authors:
Gibbons, R
,
Bachoo, S
,
Picketts, D
,
Higgs, DR
Format:
Journal article
Izdano:
1997
Zaloga
Opis
Podobne knjige/članki
Knjižničarski pogled
Opis
Izvleček:
Podobne knjige/članki
ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.
od: Picketts, D, et al.
Izdano: (1996)
Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
od: Picketts, D, et al.
Izdano: (1998)
Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.
od: Gibbons, R, et al.
Izdano: (1997)
Disruption of ATRX in mouse by conditional knockout.
od: Gibbons, R, et al.
Izdano: (2002)
Detection of mutations by RNase cleavage.
od: Watkins, H, et al.
Izdano: (2001)