Looking the cow in the eye: deletion in the NID1 gene is associated with recessive inherited cataract in Romagnola cattle.
Cataract is a known condition leading to opacification of the eye lens causing partial or total blindness. Mutations are known to cause autosomal dominant or recessive inherited forms of cataracts in humans, mice, rats, guinea pigs and dogs. The use of large-sized animal models instead of those usin...
Main Authors: | Leonardo Murgiano, Vidhya Jagannathan, Valerio Calderoni, Monika Joechler, Arcangelo Gentile, Cord Drögemüller |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2014-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0110628 |
Similar Items
-
Pseudomyotonia in Romagnola cattle caused by novel <it>ATP2A1</it> mutations
by: Murgiano Leonardo, et al.
Published: (2012-10-01) -
A Heterozygous Missense Variant in <i>MAP2K2</i> in a Stillborn Romagnola Calf with Skeletal-Cardio-Enteric Dysplasia
by: Joana G. P. Jacinto, et al.
Published: (2021-06-01) -
Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle.
by: Leonardo Murgiano, et al.
Published: (2014-01-01) -
X-Linked Duchenne-Type Muscular Dystrophy in Jack Russell Terrier Associated with a Partial Deletion of the Canine <i>DMD</i> Gene
by: Barbara Brunetti, et al.
Published: (2020-10-01) -
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
by: Bushra Irum, et al.
Published: (2016-01-01)