A Mouse Model for Meckel Syndrome Type 3

Meckel-Gruber syndrome type 3 (MKS3; OMIM 607361) is a severe autosomal recessive disorder characterized by bilateral polycystic kidney disease. Other malformations associated with MKS3 include cystic changes in the liver, polydactyly, and brain abnormalities (occipital encephalocele, hydrocephalus,...

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Detalhes bibliográficos
Main Authors: Cook, Susan A., Collin, Gayle B., Bronson, Roderick T., Naggert, Jürgen K., Liu, Dong P., Akeson, Ellen C., Davisson, Muriel T.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2009
Assuntos:
Basic Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2663826/
https://ncbi.nlm.nih.gov/pubmed/19211713
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2008040412
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