✦ LIBER ✦
Homozygosity mapping identifies a GALK1 mutation as the cause of autosomal recessive congenital cataracts in 4 adult siblings
✍ Scribed by Chacon-Camacho, Oscar F.; Buentello-Volante, Beatriz; Velázquez-Montoya, Roberto; Ayala-Ramirez, Raul; Zenteno, Juan C.
- Book ID
- 123096261
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 667 KB
- Volume
- 534
- Category
- Article
- ISSN
- 0378-1119
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