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Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers

✍ Scribed by Sharma, H.; Mavuduru, R. S.; Singh, S. K.; Prasad, R.

Book ID: 125528769
Publisher: Oxford University Press
Year: 2014
Tongue: English
Weight: 185 KB
Volume: 20
Category: Article
ISSN: 1360-9947
DOI: 10.1093/molehr/gau047

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