Evidence map›Paper›PMID 29976999›Full record

ArticleJournal of human genetics2018

Genotype-phenotype correlation in Becker muscular dystrophy in Chinese patients.

Ruiyi Yuan, Junfei Yi, Zhiying Xie, Yimeng Zheng, Miao Han, Yue Hou, Zhaoxia Wang, Yun Yuan

Abstract read
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Article in Journal of human genetics, 2018. 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
0.2field-weighted citation impact, top 47% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

8 authors at 4 institutions in 2 countries.

Ruiyi YuanDepartment of Neurology, First Hospital, Peking University, 100034, Beijing, China.
Junfei YiDepartment of Neurology, First Hospital, Peking University, 100034, Beijing, China.
Zhiying XieDepartment of Neurology, First Hospital, Peking University, 100034, Beijing, China.
Yimeng ZhengDepartment of Neurology, First Hospital, Peking University, 100034, Beijing, China.
Miao HanDepartment of Neurology, First Hospital, Henan University, Kaifeng Shi, China.
Yue HouDepartment of Neurology, Traditional Medicine Hospital, Guangzhou University, Guangzhou, China.
Zhaoxia WangDepartment of Neurology, First Hospital, Peking University, 100034, Beijing, China.
Yun YuanDepartment of Neurology, First Hospital, Peking University, 100034, Beijing, China. yuanyun2002@126.com.
Peking University · CNPeking University First Hospital · CNFirst Affiliated Hospital of Henan University · CNGuangzhou University · CN

Funding

Beijing Council of Science and Technology Z151100003915126Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2011ZX09307-001-07
6 · The paper itself

Abstract

Large deletions and duplications are the most frequent causative mutations in Becker muscular dystrophy (BMD), but genetic profile varied greatly among reports. We performed a comprehensive molecular investigation in 95 Chinese BMD patients. All patients were divided into three subtypes: normal muscle strength (type 1) in 18 cases, quadriceps myopathy (type 2) in 20 cases, and limb-girdle weakness (type 3) in 57 cases. Nineteen cases (20.0%) had small mutations and 76 cases (80.0%) had major rearrangements, including 67 cases (70.5%) of exonic deletions and 9 cases (9.5%) of exonic duplications. We identified 50 cases (65.8%) of in-frame mutations, and 26 cases (34.2%) of frame-shift mutations. The frequency of deletion in exons 13-19 was 30.6% in type 1 patients, 9.7% in type 2 patients, and 10.4% in type 3 patients. The frequency of deletion in exons 45-55 was 28.6% in type 1 patients, 40.8% in type 2, and 50.0% in type 3 patients. All major rearrangements of DMD gene in type 1 patients were also observed in type 3 patients. Our study suggested that frame-shift mutation was not rare in Chinese BMD patients. Although no difference was observed on the forms of DMD gene mutations among the three types of patients, the mutation in proximal region of DMD gene has higher frequency for patients without weakness. Effect of exon skipping for DMD depends on the size and location of the mutation. Additional studies are required to determine whether exon-skipping strategies in proximal region of DMD gene could yield more functional dystrophin.

Indexed as

MutationPhenotypeAdolescentAdultAsian PeopleChildChinaFemaleGenotypeHumansMaleMuscular Dystrophy, Duchenne

Identifiers

PMID29976999
OpenAlexW2816562378

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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.