Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses | 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 More

Article metrics

Neurogenetics

Original article

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

Online download statistics by month:

Online download statistics by month: May 2018 to December 2020

	Abstract	Full	Pdf
May 2018	614	630	48
Jun 2018	427	473	113
Jul 2018	303	303	66
Aug 2018	253	254	70
Sep 2018	158	159	55
Oct 2018	93	93	38
Nov 2018	87	87	35
Dec 2018	60	62	34
Jan 2019	79	74	27
Feb 2019	46	44	23
Mar 2019	61	59	37
Apr 2019	45	46	26
May 2019	67	66	36
Jun 2019	46	44	36
Jul 2019	65	67	22
Aug 2019	91	89	26
Sep 2019	66	63	24
Oct 2019	57	55	14
Nov 2019	58	57	28
Dec 2019	69	63	25
Jan 2020	103	95	29
Feb 2020	67	64	49
Mar 2020	78	76	28
Apr 2020	68	62	39
May 2020	64	61	46
Jun 2020	57	52	46
Jul 2020	63	54	98
Aug 2020	54	51	60
Sep 2020	50	49	42
Oct 2020	65	61	26
Nov 2020	51	49	24
Dec 2020	46	40	26
Total	3511	3502	1296