Literature DB >> 33755199

DYNC2H1 variants cause Leber congenital amaurosis without syndromic features.

Junwon Lee1, Hyunjoo Lee2, Young-Mock Lee2, Helen J Kuht3, Mervyn G Thomas3, Sang Jin Kim4, Seung-Tae Lee5, Jinu Han1.   

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Year:  2021        PMID: 33755199     DOI: 10.1111/cge.13958

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


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  1 in total

1.  TUBB3 M323V Syndrome Presents with Infantile Nystagmus.

Authors:  Soohwa Jin; Sung-Eun Park; Dongju Won; Seung-Tae Lee; Sueng-Han Han; Jinu Han
Journal:  Genes (Basel)       Date:  2021-04-15       Impact factor: 4.096

  1 in total

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