Literature DB >> 31556918

Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome.

Seung-Tae Lee1, Jinu Han2.   

Abstract

Entities:  

Year:  2019        PMID： 31556918     DOI： 10.1001/jamaophthalmol.2019.3755

Source DB:  PubMed          Journal:  JAMA Ophthalmol        ISSN： 2168-6165            Impact factor:   7.389


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  2 in total

1.  Errors in Table 2.

Authors: 
Journal:  JAMA Ophthalmol       Date:  2019-12-01       Impact factor: 7.389

2.  Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.

Authors:  Dongheon Surl; Saeam Shin; Seung-Tae Lee; Jong Rak Choi; Junwon Lee; Suk Ho Byeon; Sueng-Han Han; Hyun Taek Lim; Jinu Han
Journal:  Mol Vis       Date:  2020-02-24       Impact factor: 2.367
  2 in total

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