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Publications by Zhengmao Hu

Mutations of P4HA2 Encoding Prolyl 4-Hydroxylase 2 Are Associated With Nonsyndromic High Myopia

Genetics in Medicine
MedicineGenetics
2015English

AKAP2identified as a Novel Gene Mutated in a Chinese Family With Adolescent Idiopathic Scoliosis

Journal of Medical Genetics
Genetics
2016English

A Novel Locus for Congenital Simple Microphthalmia Family Mapping to 17p12-Q12

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2011English

Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population

Frontiers in Neurology
Neurology
2018English

Hutchinson-Gilford Progeria Syndrome Accompanied by Severe Skeletal Abnormalities in Two Chinese Siblings: Two Case Reports

Journal of Medical Case Reports
Medicine
2013English

Altered Gut Microbiome in Autism Spectrum Disorder: Potential Mechanism and Implications for Clinical Intervention

Global Clinical and Translational Research
2019English

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