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A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

Chromosome structural changes with nonrecurrent endpoints associated with genomic disorders offer windows into the mechanism of origin of copy number variation (CNV). A recent report of nonrecurrent duplications associated with Pelizaeus-Merzbacher disease identified three distinctive characteristic...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Hastings, P. J., Ira, Grzegorz, Lupski, James R.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Public Library of Science 2009
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC2621351/
https://ncbi.nlm.nih.gov/pubmed/19180184
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000327
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