Mutations in the y2 subunit of AMP-activated protein kinase case familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

E Blair; C Redwood; H Ashrafian; M Oliveira; J Brotholme; B Kerr; A Salmon; I Ostman-Smith; H. Watkins

Mutations in the y2 subunit of AMP-activated protein kinase case familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

E Blair, C Redwood, H Ashrafian, M Oliveira, J Brotholme, B Kerr, A Salmon, I Ostman-Smith, H. Watkins

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

Original language	English
Journal	Human Molecular Genetics
Volume	10
Publication status	Published - 2001

Cite this

@article{a1cbd99ef4134a63946d088803b595d1,

title = "Mutations in the y2 subunit of AMP-activated protein kinase case familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis",

author = "E Blair and C Redwood and H Ashrafian and M Oliveira and J Brotholme and B Kerr and A Salmon and I Ostman-Smith and H. Watkins",

year = "2001",

language = "English",

volume = "10",

journal = "Human Molecular Genetics",

issn = "1460-2083",

publisher = "Oxford University Press",

}

TY - JOUR

T1 - Mutations in the y2 subunit of AMP-activated protein kinase case familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

AU - Blair, E

AU - Redwood, C

AU - Ashrafian, H

AU - Oliveira, M

AU - Brotholme, J

AU - Kerr, B

AU - Salmon, A

AU - Ostman-Smith, I

AU - Watkins, H.

PY - 2001

Y1 - 2001

M3 - Article

SN - 1460-2083

VL - 10

JO - Human Molecular Genetics

JF - Human Molecular Genetics

ER -