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Corrigendum: Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017–2022

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Juan Zhang
Rui Yang
Dayong Zhang
Ming Wang
Chaowen Yu
Jingli Yang
Wenxia Huang
Shan Liu
Shi Tang

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doi 10.3389/fgene.2024.1449534

454 views

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in Genetics of Common and Rare Diseases

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doi 10.3389/fgene.2024.1430703

733 views

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Published on 25 Jun 2024

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in Genetics of Common and Rare Diseases

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Jihene Marrakchi
Nessrine Mezzi
Lilia Romdhane
Maroua Boujemaa
Hamza Dallali
Marwa Sayeb
Saida Lahbib
Hajer Jaouadi

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doi 10.3389/fgene.2024.1437233

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Yanling Teng
Wen Zhang
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Desheng Liang
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doi 10.3389/fgene.2024.1415811

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in Genetics of Common and Rare Diseases

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doi 10.3389/fgene.2024.1377237

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in Genetics of Common and Rare Diseases

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Melania Abreu-González
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doi 10.3389/fgene.2024.1430414

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in Genetics of Common and Rare Diseases

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Xiangyu Zhu
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Na Kong

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doi 10.3389/fgene.2024.1407202

781 views

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doi 10.3389/fgene.2024.1375736

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A novel insertional allele of the CG18135 gene is associated with severe mutant phenotypes in Drosophila melanogaster

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doi 10.3389/fgene.2024.1355368

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in Genetics of Common and Rare Diseases

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Lu Wang
Jiahe Yu
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doi 10.3389/fgene.2024.1409226

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Jiang Yuqing
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doi 10.3389/fgene.2024.1387598

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Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience

in Genetics of Common and Rare Diseases

Dongming Li
Lifang Liang
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Navigation group

Articles

Corrigendum: Disease spectrum, prevalence, genetic characteristics of inborn errors of metabolism in 21,840 hospitalized infants in Chongqing, China, 2017–2022

Editorial: Neuronal ceroid lipofuscinosis: molecular genetics and epigenetics

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

Application of whole exome sequencing in carrier screening for high-risk families without probands

How does the age of control individuals hinder the identification of target genes for Huntington’s disease?

Editorial: Inborn errors of carbohydrate metabolism

ZP1-Y262C mutation causes abnormal zona pellucida formation and female infertility in humans

Deciphering the pathogenic role of rare RAF1 heterozygous missense mutation in the late-presenting DDH

A novel insertional allele of the CG18135 gene is associated with severe mutant phenotypes in Drosophila melanogaster

Clinical profiles and molecular genetic analyses of 98 Chinese children with short statures

Revealing the genetic complexity of hypothyroidism: integrating complementary association methods

Identification of oxidative phosphorylation-related genes in moyamoya disease by combining bulk RNA-sequencing analysis and machine learning

Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants

Rare exonic CELSR3 variants identified in Bladder Exstrophy Epispadias Complex

A novel IRF6 gene mutation impacting the regulation of TGFβ2-AS1 in the TGFβ pathway: A mechanism in the development of Van der Woude syndrome

Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience