When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)-Reference-Cited by-同舟云学术

When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)

Published:2020-03-30 Issue:7 Volume:65 Page:609-617
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Mohseni Marzieh,Akbari Mojdeh,Booth Kevin T.,Babanejad Mojgan,Azaiez Hela,Ardalani Fariba,Arzhangi Sanaz,Jalalvand Khadijeh,Nikzat Nooshin,Ghodratpour Fatemeh,Jamali Payman,Adeli Omid Ali,Habibi Haleh,Kahrizi Kimia,Najmabadi Hossein

Funder

Iran National Science Foundation

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s10038-020-0740-z.pdf

Reference40 articles.

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3. Mocciaro A, Berdougo E, Zeng K, Black E, Vagnarelli P, Earnshaw W, et al. Vertebrate cells genetically deficient for Cdc14A or Cdc14B retain DNA damage checkpoint proficiency but are impaired in DNA repair. J Cell Biol. 2010;189:631–9.

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