A closed gap junction channel state caused by a single site mutation in the 3rd transmembrane helix

D. L. Beahm; G. G. Gaietta; A. Chandrasekhar; G. M. Hand; A. Smock; A. Oshima; B. J. Nicholson; G. E. Sosinsky

doi:10.1017/S1431927604887348

A closed gap junction channel state caused by a single site mutation in the 3^rd transmembrane helix

D. L. Beahm
, G. G. Gaietta
, A. Chandrasekhar
, G. M. Hand
, A. Smock
, A. Oshima
, B. J. Nicholson
, G. E. Sosinsky

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

Original language	English (US)
Pages (from-to)	1498-1499
Number of pages	2
Journal	Microscopy and Microanalysis
Volume	10
Issue number	SUPPL. 2
DOIs	https://doi.org/10.1017/S1431927604887348
State	Published - 2004
Externally published	Yes

ASJC Scopus subject areas

Instrumentation

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10.1017/S1431927604887348

Cite this

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title = "A closed gap junction channel state caused by a single site mutation in the 3rd transmembrane helix",

author = "Beahm, \{D. L.\} and Gaietta, \{G. G.\} and A. Chandrasekhar and Hand, \{G. M.\} and A. Smock and A. Oshima and Nicholson, \{B. J.\} and Sosinsky, \{G. E.\}",

year = "2004",

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volume = "10",

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publisher = "Oxford University Press",

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T1 - A closed gap junction channel state caused by a single site mutation in the 3rd transmembrane helix

AU - Beahm, D. L.

AU - Gaietta, G. G.

AU - Chandrasekhar, A.

AU - Hand, G. M.

AU - Smock, A.

AU - Oshima, A.

AU - Nicholson, B. J.

AU - Sosinsky, G. E.

PY - 2004

Y1 - 2004

UR - https://www.scopus.com/pages/publications/4544234166

UR - https://www.scopus.com/pages/publications/4544234166#tab=citedBy

U2 - 10.1017/S1431927604887348

DO - 10.1017/S1431927604887348

M3 - Article

AN - SCOPUS:4544234166

SN - 1431-9276

VL - 10

SP - 1498

EP - 1499

JO - Microscopy and Microanalysis

JF - Microscopy and Microanalysis

IS - SUPPL. 2

ER -

A closed gap junction channel state caused by a single site mutation in the 3rd transmembrane helix

ASJC Scopus subject areas

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A closed gap junction channel state caused by a single site mutation in the 3^rd transmembrane helix