A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.

Mutations in the ATRX gene cause a severe X-linked mental retardation syndrome that is frequently associated with alpha thalassemia (ATR-X syndrome). The previously characterized ATRX protein (approximately 280 kDa) contains both a Plant homeodomain (PHD)-like zinc finger motif as well as an ATPase...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखकों: Garrick, D, Samara, V, McDowell, T, Smith, A, Dobbie, L, Higgs, D, Gibbons, R
स्वरूप: Journal article
भाषा:English
प्रकाशित: 2004