U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

Links from MedGen

Items: 4

1.
A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss
Ghulam Mujtaba, Julie M Schultz, Ayesha Imtiaz, Robert J Morell, Thomas B Friedman, Sadaf Naz
J Med Genet. Author manuscript; available in PMC 2016 Aug 1.
Published in final edited form as: J Med Genet. 2015 Aug; 52(8): 548–552. Published online 2015 May 4. doi: 10.1136/jmedgenet-2015-103023
PMCID:
PMC4529444
ArticlePDF–391K
2.
Hepatocyte Growth Factor–c-MET Signaling Mediates the Development of Nonsensory Structures of the Mammalian Cochlea and Hearing
Shumei Shibata, Toru Miwa, Hsiao-Huei Wu, Pat Levitt, Takahiro Ohyama
J Neurosci. 2016 Aug 3; 36(31): 8200–8209. doi: 10.1523/JNEUROSCI.4410-15.2016
PMCID:
PMC4971366
ArticlePDF–4.8M
3.
Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype
Carina Frykholm, Joakim Klar, Tatjana Tomanovic, Adam Ameur, Niklas Dahl
Eur J Hum Genet. 2018 Dec; 26(12): 1871–1874. Published online 2018 Sep 24. doi: 10.1038/s41431-018-0256-6
PMCID:
PMC6244415
ArticlePDF–729K
4.
Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis
Ya-Jie Lu, Jun Yao, Qin-Jun Wei, Guang-Qian Xing, Xin Cao
Medicine (Baltimore) 2015 Dec; 94(50): e2248. Published online 2015 Dec 18. doi: 10.1097/MD.0000000000002248
PMCID:
PMC5058913
ArticlePDF–690K

Display Settings:

Format
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center