Evidence map›Paper›PMID 9246005›Full record

ArticleAmerican journal of human genetics1997

DNA studies of limb-girdle muscular dystrophy type 2A in the Amish exclude a modifying mitochondrial gene and show no evidence for a modifying nuclear gene.

V M Pratt, C E Jackson, D C Wallace, D S Gurley, A Feit, G L Feldman

Open access · bronzeAbstract readLetter
In one paragraph

Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

V M Pratt
C E Jackson
D C Wallace
D S Gurley
A Feit
G L Feldman
Henry Ford Hospital · USEmory University · US

Funding

MITOCHONDRIAL INBORN ERRORS OF METABOLISMR01NS021328 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI WALLACE, DOUGLAS C · 1985 to 2017
$6.5M
MITOCHONDRIAL GENES AND CARDIOVASCULAR DISEASESR01HL045572 · NHLBI · EMORY UNIVERSITY · PI WALLACE, DOUGLAS C · 1991 to 1998
–
NHLBI NIH HHS HL45572NINDS NIH HHS NS21328
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ChildChromosomes, Human, Pair 15DNADNA, MitochondrialFemaleHumansIndianaMaleMuscular DystrophiesDNADNA, Mitochondrial

Identifiers

PMID9246005
PMCPMC1715865
OpenAlexW1966755927

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.