Literature DB >> 19659471

Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation.

J K Gass1, N J Wilson, F J D Smith, E B Lane, W H I McLean, E Rytina, I Salvary, N P Burrows.   

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Year:  2009        PMID： 19659471     DOI： 10.1111/j.1365-2133.2009.09383.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


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  4 in total

Review 1.  Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.

Authors:  Sabine Ruf; Dana Klimas; Mario Hönemann; Sarah Jabir
Journal:  J Orofac Orthop       Date:  2013-07-05       Impact factor: 1.938

2.  Steatocystoma multiplex-a rare genetic disorder: a case report and review of the literature.

Authors:  Hemlata T Kamra; Pradeep A Gadgil; Ajay G Ovhal; Rahul R Narkhede
Journal:  J Clin Diagn Res       Date:  2013-01-01

3.  Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.

Authors:  Gül Keskin; Kadri Karaer; Zübeyde Uçar Gündoğar
Journal:  J Orofac Orthop       Date:  2021-03-16       Impact factor: 2.341

4.  Steatocystoma multiplex is associated with the R94C mutation in the KRTl7 gene.

Authors:  Qiao Liu; Weiwei Wu; Jiejie Lu; Ping Wang; Feng Qiao
Journal:  Mol Med Rep       Date:  2015-07-08       Impact factor: 2.952
  4 in total

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