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Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis

✍ Scribed by Campeau, P. M.; Lu, J. T.; Sule, G.; Jiang, M.-M.; Bae, Y.; Madan, S.; Hogler, W.; Shaw, N. J.; Mumm, S.; Gibbs, R. A.; Whyte, M. P.; Lee, B. H.

Book ID: 125474227
Publisher: Oxford University Press
Year: 2012
Tongue: English
Weight: 262 KB
Volume: 21
Category: Article
ISSN: 0964-6906
DOI: 10.1093/hmg/dds326

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