A Novel Autosomal Recessive GJA1 Missense Mutation Linked to Craniometaphyseal Dysplasia

Craniometaphyseal dysplasia (CMD) is a rare sclerosing skeletal disorder with progressive hyperostosis of craniofacial bones. CMD can be inherited in an autosomal dominant (AD) trait or occur after de novo mutations in the pyrophosphate transporter ANKH. Although the autosomal recessive (AR) form of...

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Detalles Bibliográficos
Autores principales: Hu, Ying, Chen, I-Ping, de Almeida, Salome, Tiziani, Valdenize, Do Amaral, Cassio M. Raposo, Gowrishankar, Kalpana, Passos-Bueno, Maria Rita, Reichenberger, Ernst J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3741164/
https://www.ncbi.nlm.nih.gov/pubmed/23951358
http://dx.doi.org/10.1371/journal.pone.0073576

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3741164/
https://www.ncbi.nlm.nih.gov/pubmed/23951358
http://dx.doi.org/10.1371/journal.pone.0073576

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