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Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1

✍ Scribed by Prokudin, Ivan; Simons, Cas; Grigg, John R; Storen, Rebecca; Kumar, Vikrant; Phua, Zai Y; Smith, James; Flaherty, Maree; Davila, Sonia; Jamieson, Robyn V


Book ID
124166498
Publisher
Nature Publishing Group
Year
2013
Tongue
English
Weight
648 KB
Volume
22
Category
Article
ISSN
1018-4813

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