Evidence map›Paper›PMID 7825579›Full record

ArticleAmerican journal of human genetics1995

Refinement of the spinal muscular atrophy locus by genetic and physical mapping.

C H Wang, P W Kleyn, E Vitale, B M Ross, L Lien, J Xu, T A Carter, L M Brzustowicz, S Obici, S Selig

Abstract read
In one paragraph

Article in American journal of human genetics, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.Proceedings of the National Academy of Sciences of the United States of America · 1995
    Article
  6. Article
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

10 authors.

C H WangDepartment of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032.
P W Kleyn
E Vitale
B M Ross
L Lien
J Xu
T A Carter
L M Brzustowicz
S Obici
S Selig

Funding

MOLECULAR GENETICS OF DUCHENNE MUSCULAR DYSTROPHYR01NS023740 · NINDS · CHILDREN'S HOSPITAL BOSTON · PI KUNKEL, LOUIS M · 1986 to 1997
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SPINAL MUSCULAR ATROPHY--GENE MAPPING &CHARACTERIZATIONR01NS028877 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI GILLIAM, THOMAS CONRAD · 1990 to 1997
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NINDS NIH HHS NS23740NINDS NIH HHS NS28877NINDS NIH HHS NSO1576
6 · The paper itself

Abstract

We report the mapping and characterization of 12 microsatellite markers including 11 novel markers. All markers were generated from overlapping YAC clones that span the spinal muscular atrophy (SMA) locus. PCR amplification of 32 overlapping YAC clones shows that 9 of the new markers (those set in italics) map to the interval between the two previous closest flanking markers (D5S629 and D5S557): cen-D5S6-D5S125-D5S435-D5S1407- D5S629-D5S1410-D5S1411/D5S1412-D5S1413- D5S1414-D5Z8-D5Z9-CATT1-D5Z10/D5Z6- D5S557-D5S1408-D5S1409-D5S637-D5S351-MA P1B-tel. Four of these new markers detect multiple loci in and out of the SMA gene region. Genetic analysis of recombinant SMA families indicates that D5S1413 is a new proximal flanking locus for the SMA gene. Interestingly, among the 40 physically mapped loci, the 14 multilocus markers map contiguously to a genomic region that overlaps, and perhaps helps define, the minimum genetic region encompassing the SMA gene(s).

Indexed as

Chromosomes, Human, Pair 5Base SequenceChild, PreschoolChromosome MappingChromosomes, Artificial, YeastColiphagesCosmidsDNA, SatelliteFemaleGenetic MarkersHumansInfantMolecular Sequence DataMuscular Atrophy, SpinalPedigreeSpinal Muscular Atrophies of ChildhoodDNA, SatelliteGenetic Markers

Identifiers

PMID7825579
PMCPMC1801348

What OpenQuestion holds

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Registered trials

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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.