The D90A mutation results in a polymorphism of Cu, Zn superoxide dismutase that is prevalent in northern Sweden and finland

A. Själander; G. Beckman; H. X. Deng; Z. Lqbal; J. A. Tainer; T. Siddique

doi:10.1093/hmg/4.6.1105

The D90A mutation results in a polymorphism of Cu, Zn superoxide dismutase that is prevalent in northern Sweden and finland

A. Själander, G. Beckman, H. X. Deng, Z. Lqbal, J. A. Tainer, T. Siddique^*

^*Corresponding author for this work

Neurology

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

38 Scopus citations

Original language	English (US)
Pages (from-to)	1105-1108
Number of pages	4
Journal	Human molecular genetics
Volume	4
Issue number	6
DOIs	https://doi.org/10.1093/hmg/4.6.1105
State	Published - Jun 1995

ASJC Scopus subject areas

Molecular Biology
Genetics
Genetics(clinical)

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@article{ef93dda82ebc4586aea50d86f33be767,

title = "The D90A mutation results in a polymorphism of Cu, Zn superoxide dismutase that is prevalent in northern Sweden and finland",

author = "A. Sj{\"a}lander and G. Beckman and Deng, {H. X.} and Z. Lqbal and Tainer, {J. A.} and T. Siddique",

note = "Funding Information: We are grateful to the families who participated in this study. We thank Annette Lyles for her assistance in preparing the manuscript. This work was supported by the National Institutes of Neurological Disorders and Stroke (T.S., H.-X.D.), Les Turner ALS Foundation (T.S.), Searle Family Center for Neurological Disorders (T.S.), the N1GMS (J.A.T.), Vena E.Schaaf ALS Research Fund (T.S.), Muriel Heller ALS Fellowship (W.-Y.H.), The Gisela Fund for ALS Research (T.S.), The Muscular Dystrophy Association of America (Z.I.) and The Herbert & Florence C.Wenske Foundation (T.S.).",

year = "1995",

month = jun,

doi = "10.1093/hmg/4.6.1105",

language = "English (US)",

volume = "4",

pages = "1105--1108",

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TY - JOUR

T1 - The D90A mutation results in a polymorphism of Cu, Zn superoxide dismutase that is prevalent in northern Sweden and finland

AU - Själander, A.

AU - Beckman, G.

AU - Deng, H. X.

AU - Lqbal, Z.

AU - Tainer, J. A.

AU - Siddique, T.

N1 - Funding Information: We are grateful to the families who participated in this study. We thank Annette Lyles for her assistance in preparing the manuscript. This work was supported by the National Institutes of Neurological Disorders and Stroke (T.S., H.-X.D.), Les Turner ALS Foundation (T.S.), Searle Family Center for Neurological Disorders (T.S.), the N1GMS (J.A.T.), Vena E.Schaaf ALS Research Fund (T.S.), Muriel Heller ALS Fellowship (W.-Y.H.), The Gisela Fund for ALS Research (T.S.), The Muscular Dystrophy Association of America (Z.I.) and The Herbert & Florence C.Wenske Foundation (T.S.).

PY - 1995/6

Y1 - 1995/6

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U2 - 10.1093/hmg/4.6.1105

DO - 10.1093/hmg/4.6.1105

M3 - Article

C2 - 7655469

AN - SCOPUS:0029066863

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JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 6

ER -

The D90A mutation results in a polymorphism of Cu, Zn superoxide dismutase that is prevalent in northern Sweden and finland

ASJC Scopus subject areas

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