Literature DB >> 26087145

Missense and deletion mutations in GJA1 causing oculodentodigital dysplasia in two Indian families.

Abhilash Dwarakanathan1, Meenakshi Bhat, Sanjeeva Gn, Swathi Shetty.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2015        PMID： 26087145     DOI： 10.1097/MCD.0000000000000094

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


× No keyword cloud information.
  2 in total

1.  Oculodentodigital Dysplasia Presenting as Spastic Paraparesis: The First Genetically Confirmed Korean Case and a Literature Review.

Authors:  Kye Won Park; Ho-Sung Ryu; Juyeon Kim; Sun Ju Chung
Journal:  J Mov Disord       Date:  2017-09-22

2.  Oculodentodigital Dysplasia: A Case Report and Major Review of the Eye and Ocular Adnexa Features of 295 Reported Cases.

Authors:  Virang Kumar; Natario L Couser; Arti Pandya
Journal:  Case Rep Ophthalmol Med       Date:  2020-04-04
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.