A novel 5 nucleotide deletion in XPA gene is associated with severe neurological abnormalities.
about
XPA: A key scaffold for human nucleotide excision repair.Genetic investigation of XPA gene: high frequency of the c.682C>T mutation in Moroccan XP patients with moderate clinical profile.Structural dynamics and interactions of Xeroderma pigmentosum complementation group A (XPA98-210) with damaged DNA.
P2860
A novel 5 nucleotide deletion in XPA gene is associated with severe neurological abnormalities.
description
2015 nî lūn-bûn
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2015年学术文章
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name
A novel 5 nucleotide deletion ...... re neurological abnormalities.
@en
A novel 5 nucleotide deletion ...... re neurological abnormalities.
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type
label
A novel 5 nucleotide deletion ...... re neurological abnormalities.
@en
A novel 5 nucleotide deletion ...... re neurological abnormalities.
@nl
prefLabel
A novel 5 nucleotide deletion ...... re neurological abnormalities.
@en
A novel 5 nucleotide deletion ...... re neurological abnormalities.
@nl
P2093
P50
P1433
P1476
A novel 5 nucleotide deletion ...... ere neurological abnormalities
@en
P2093
Majid Fardaei
Mohammad Miryounesi
Soudeh Ghafouri-Fard
P304
P356
10.1016/J.GENE.2015.08.039
P407
P433
P577
2015-08-21T00:00:00Z