Phenotypic and molecular insights into CASK-related disorders in males

BACKGROUND: Heterozygous loss-of-function mutations in the X-linked CASK gene cause progressive microcephaly with pontine and cerebellar hypoplasia (MICPCH) and severe intellectual disability (ID) in females. Different CASK mutations have also been reported in males. The associated phenotypes range...

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Detalles Bibliográficos
Autores principales: Moog, Ute, Bierhals, Tatjana, Brand, Kristina, Bautsch, Jan, Biskup, Saskia, Brune, Thomas, Denecke, Jonas, de Die-Smulders, Christine E, Evers, Christina, Hempel, Maja, Henneke, Marco, Yntema, Helger, Menten, Björn, Pietz, Joachim, Pfundt, Rolph, Schmidtke, Jörg, Steinemann, Doris, Stumpel, Constance T, Van Maldergem, Lionel, Kutsche, Kerstin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449965/
https://www.ncbi.nlm.nih.gov/pubmed/25886057
http://dx.doi.org/10.1186/s13023-015-0256-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4449965/
https://www.ncbi.nlm.nih.gov/pubmed/25886057
http://dx.doi.org/10.1186/s13023-015-0256-3

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