Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction

R. Witoonpanich; T. Pulkes; C. Dejthevaporn; P. Witoonpanich; P. Yodnopklao; S. Wetchaphanphesat; J. Brengman; A. G. Engel

doi:10.1016/j.nmd.2012.02.001

Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction

R. Witoonpanich, T. Pulkes, C. Dejthevaporn, P. Witoonpanich, P. Yodnopklao, S. Wetchaphanphesat, J. Brengman, A. G. Engel

Neurology

Research output: Contribution to journal › Letter › peer-review

1 Scopus citations

Original language	English (US)
Pages (from-to)	478
Number of pages	1
Journal	Neuromuscular Disorders
Volume	22
Issue number	5
DOIs	https://doi.org/10.1016/j.nmd.2012.02.001
State	Published - May 2012

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Neurology
Clinical Neurology
Genetics(clinical)

Access to Document

10.1016/j.nmd.2012.02.001

Cite this

@article{2eec67e5d85143f895712dfa72f72025,

title = "Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction",

author = "R. Witoonpanich and T. Pulkes and C. Dejthevaporn and P. Witoonpanich and P. Yodnopklao and S. Wetchaphanphesat and J. Brengman and Engel, {A. G.}",

year = "2012",

month = may,

doi = "10.1016/j.nmd.2012.02.001",

language = "English (US)",

volume = "22",

pages = "478",

journal = "Neuromuscular Disorders",

issn = "0960-8966",

publisher = "Elsevier Limited",

number = "5",

}

TY - JOUR

T1 - Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship

T2 - Correction

AU - Witoonpanich, R.

AU - Pulkes, T.

AU - Dejthevaporn, C.

AU - Witoonpanich, P.

AU - Yodnopklao, P.

AU - Wetchaphanphesat, S.

AU - Brengman, J.

AU - Engel, A. G.

PY - 2012/5

Y1 - 2012/5

UR - http://www.scopus.com/inward/record.url?scp=84859627986&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84859627986&partnerID=8YFLogxK

U2 - 10.1016/j.nmd.2012.02.001

DO - 10.1016/j.nmd.2012.02.001

M3 - Letter

C2 - 22406191

AN - SCOPUS:84859627986

SN - 0960-8966

VL - 22

SP - 478

JO - Neuromuscular Disorders

JF - Neuromuscular Disorders

IS - 5

ER -

Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this