Literature DB >> 18383610

Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency.

Kunal Ray1, Moumita Chaki, Mainak Sengupta.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2007        PMID： 18383610

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


× No keyword cloud information.
  1 in total

1.  Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism.

Authors:  Jung Min Ko; Jung-Ah Yang; Seon-Yong Jeong; Hyon-Ju Kim
Journal:  Mol Med Rep       Date:  2012-01-25       Impact factor: 2.952
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.