Identification of a 31-bp Deletion in the RELN Gene Causing Lissencephaly with Cerebellar Hypoplasia in Sheep

Lissencephaly is an inherited developmental disorder in which neuronal migration is impaired. A type of lissencephaly associated with cerebellar hypoplasia (LCH) was diagnosed in a commercial flock of Spanish Churra sheep. The genotyping of 7 affected animals and 33 controls with the OvineSNP50 Bead...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Suárez-Vega, Aroa, Gutiérrez-Gil, Beatriz, Cuchillo-Ibáñez, Inmaculada, Sáez-Valero, Javier, Pérez, Valentín, García-Gámez, Elsa, Benavides, Julio, Arranz, Juan Jose
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2013
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3834269/
https://ncbi.nlm.nih.gov/pubmed/24260534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0081072
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