Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
about
An abundant evolutionarily conserved CSB-PiggyBac fusion protein expressed in Cockayne syndromeEarly postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genesThe case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum.Progeroid syndromes: probing the molecular basis of aging?Genetic correction of stem cells in the treatment of inherited diseases and focus on xeroderma pigmentosum.UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I.
P2860
Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
description
1992 nî lūn-bûn
@nan
1992 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@ast
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@en
type
label
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@ast
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@en
prefLabel
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@ast
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@en
P2093
P2860
P1476
Xeroderma pigmentosum and Cock ...... al and biochemical phenotypes.
@en
P2093
Cleaver JE
Duke-Woodside ME
Greenhaw GA
P2860
P304
P407
P577
1992-04-01T00:00:00Z