A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesis
Author:
Funder
Ministry of Education – Kingdom of Saudi Arabi
Publisher
Elsevier BV
Subject
Cell Biology,General Dentistry,General Medicine,Otorhinolaryngology
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3. Identification of potential key variants in mandibular premolar hypodontia through whole-exome sequencing;Frontiers in Genetics;2023-09-08
4. Novel MSX1 variants identified in families with nonsyndromic oligodontia;International Journal of Oral Science;2021-01-08
5. A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontia;Annals of Human Genetics;2019-08-30
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