Rising of LOXHD1 as a signature causative gene of down-sloping hearing loss in people in their teens and 20s | Journal of Medical Genetics

Subscribe
Log In More

Log in via Institution
Log in via OpenAthens
Log in via CCMG

Log in using your username and password
For personal accounts OR managers of institutional accounts

Username *

Password *

Forgot your log in details?Register a new account?
Forgot your user name or password?
Basket
Search More

Search for this keyword

Advanced search

Close More
Main menu

Latest content

Current issue

Archive

Authors

About
Subscribe
Log in More

Log in via Institution
Log in via OpenAthens
Log in via CCMG

Log in using your username and password
For personal accounts OR managers of institutional accounts

Username *

Password *

Forgot your log in details?Register a new account?
Forgot your user name or password?
BMJ Journals

Article metrics

Genotype-phenotype correlations

Original research

Rising of LOXHD1 as a signature causative gene of down-sloping hearing loss in people in their teens and 20s

Online download statistics by month:

Online download statistics by month: March 2021 to February 2023

	Abstract	Full	Pdf
Mar 2021	607	38	24
Apr 2021	448	16	11
May 2021	109	23	1
Jun 2021	5	5	0
Jul 2021	13	10	5
Aug 2021	19	16	7
Sep 2021	10	10	3
Oct 2021	120	3	1
Nov 2021	205	2	1
Dec 2021	128	10	7
Jan 2022	278	12	10
Feb 2022	147	3	5
Mar 2022	141	10	5
Apr 2022	391	13	12
May 2022	367	36	15
Jun 2022	150	31	8
Jul 2022	141	17	4
Aug 2022	109	7	0
Sep 2022	105	10	3
Oct 2022	155	18	9
Nov 2022	190	12	6
Dec 2022	93	18	8
Jan 2023	166	11	6
Feb 2023	79	9	10
Total	4176	340	161