A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family.

Möbius syndrome (MIM 157900) consists of a congenital paresis or paralysis of the VIIth (facial) cranial nerve, frequently accompanied by dysfunction of other cranial nerves. The abducens nerve is typically affected, and often, also, the hypoglossal nerve. In addition, orofacial and limb malformatio...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Verzijl, H T, van den Helm, B, Veldman, B, Hamel, B C, Kuyt, L P, Padberg, G W, Kremer, H
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1999
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377982/
https://ncbi.nlm.nih.gov/pubmed/10441582
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