Phenotype and Variant Spectrum in the LAMB3 Form of Amelogenesis Imperfecta

Amelogenesis imperfecta (AI) is a heterogeneous group of inherited disorders characterized by abnormal formation of dental enamel, either in isolation or as part of a syndrome. Heterozygous variants in laminin subunit beta 3 (LAMB3) cause AI with dominant inheritance in the absence of other cosegreg...

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Dades bibliogràfiques
Publicat a:J Dent Res
Autors principals: Smith, C.E.L., Poulter, J.A., Brookes, S.J., Murillo, G., Silva, S., Brown, C.J., Patel, A., Hussain, H., Kirkham, J., Inglehearn, C.F., Mighell, A.J.
Format: Artigo
Idioma:Inglês
Publicat: SAGE Publications 2019
Matèries:
Research Reports
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6535922/
https://ncbi.nlm.nih.gov/pubmed/30905256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034519835205
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