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Evidence for additional FREM1 heterogeneity in Manitoba oculotrichoanal syndrome

PURPOSE: Manitoba Oculotrichoanal (MOTA) syndrome is an autosomal recessive disorder present in First Nations families that is characterized by ocular (cryptophthalmos), facial, and genital anomalies. At the commencement of this study, its genetic basis was undefined. METHODS: Homozygosity analysis...

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Detalhes bibliográficos
Main Authors: Mateo, Robertino Karlo, Johnson, Royce, Lehmann, Ordan J.
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3369896/
https://ncbi.nlm.nih.gov/pubmed/22690109
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