Evidence map›Paper›PMID 25681079›Full record

ArticleJIMD reports2015

A De Novo Variant in Galactose-1-P Uridylyltransferase (GALT) Leading to Classic Galactosemia.

Thanh-Thanh Claire V Tran, Ying Liu, Michael E Zwick, Dhanya Ramachandran, David J Cutler, Xiaoping Huang, Gerard T Berry, Judith L Fridovich-Keil

Open access · bronzeAbstract read
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Article in JIMD reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
–field-weighted citation impact, top 90% 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

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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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Thanh-Thanh Claire V TranBiology Department, Emory College, Emory University, Atlanta, GA, 30322, USA.
Ying Liu
Michael E Zwick
Dhanya Ramachandran
David J Cutler
Xiaoping Huang
Gerard T Berry
Judith L Fridovich-Keil
Emory University · USBoston Children's Hospital · USDana-Farber/Boston Children's Cancer and Blood Disorders Center · US

Funding

Studies of Galactose Toxicity in Yeast and Human CellsR01DK059904 · NIDDK · EMORY UNIVERSITY · PI FRIDOVICH-KEIL, JUDITH L. · 2002 to 2011
$3.2M
Training Program in Human Disease GeneticsT32MH087977 · NIMH · EMORY UNIVERSITY · PI WARREN, STEPHEN T. · 2009 to 2013
$1.3M
NIDDK NIH HHS R01 DK059904NIMH NIH HHS T32 MH087977
6 · The paper itself

Abstract

Classic galactosemia (CG) is a potentially lethal genetic disease that results from profound impairment of galactose-1-P uridylyltransferase (GALT), the middle enzyme in the Leloir pathway of galactose metabolism. Patients with CG carry pathogenic loss-of-function mutations in both of their GALT alleles; the parents of patients are considered obligate carriers. We report here a first exception to that rule - a de novo GALT variant in a patient with classic galactosemia. The new variant, c.563A>C (p.Q188P), which introduces a missense substitution near the active site of the GALT enzyme, was found in the compound heterozygous state in a child with classic galactosemia, but not in either of her parents. Extensive genomic studies of DNA from the child and both parents confirmed the expected degrees of relationship in the trio as well as inheritance of a common c.563A>G (p.Q188R) GALT mutation from the mother. This result demonstrates that not all pathogenic GALT mutations are inherited and raises concern that GALT may have a higher new mutation rate than previously believed.

Identifiers

PMID25681079
PMCPMC4501235
OpenAlexW1479862173

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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.