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.
Emerging roles of TRIO and F-actin-binding protein in human diseases
Sungjin Park, Hyunji Lee, Minhee Kim, Jisoo Park, Seon-Hwan Kim, Jongsun Park
Cell Commun Signal. 2018; 16: 29. Published online 2018 Jun 11. doi: 10.1186/s12964-018-0237-y
PMCID:
PMC5996455
ArticlePDF–1.1M
2.
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes
K. Sigvard Olsson, Olof Wålinder, Ulf Jansson, Maria Wilbe, Marie-Louise Bondeson, Eva-Lena Stattin, Ruma Raha-Chowdhury, Roger Williams
Hereditas. 2017; 154: 16. Published online 2017 Dec 19. doi: 10.1186/s41065-017-0052-2
PMCID:
PMC5735936
ArticlePDF–1.1M
3.
Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction
Hiroshi Nakanishi, Kiyoto Kurima, Yoshiyuki Kawashima, Andrew J. Griffith
Auris Nasus Larynx. Author manuscript; available in PMC 2015 Oct 1.
Published in final edited form as: Auris Nasus Larynx. 2014 Oct; 41(5): 399–408. Published online 2014 Jun 2. doi: 10.1016/j.anl.2014.04.001
PMCID:
PMC4176506
ArticlePDF–211K
4.
Mutation Analysis of SLC26A4 for Pendred Syndrome and Nonsyndromic Hearing Loss by High-Resolution Melting
Neng Chen, Lisbeth Tranebjærg, Nanna Dahl Rendtorff, Iris Schrijver
J Mol Diagn. 2011 Jul; 13(4): 416–426. doi: 10.1016/j.jmoldx.2011.03.003
PMCID:
PMC3123795
ArticlePDF–1.2M

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