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Mutations in TMEM231 cause Meckel–Gruber syndrome

BACKGROUND: Meckel–Gruber syndrome (MKS) is a genetically heterogeneous severe ciliopathy characterised by early lethality, occipital encephalocele, polydactyly, and polycystic kidney disease. PURPOSE: To report genetic analysis results in two families in which all known MKS diseases genes have been...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Shaheen, Ranad, Ansari, Shinu, Mardawi, Elham AL, Alshammari, Muneera J, Alkuraya, Fowzan S
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Publishing Group 2013
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3585488/
https://ncbi.nlm.nih.gov/pubmed/23349226
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2012-101431
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