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Publications by Mz Piao
Arg555Gln Mutation of TGFBI Gene in Geographical-Type Reis—Bücklers Corneal Dystrophy in a Chinese Family
Journal of International Medical Research
Biochemistry
Medicine
Cell Biology
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A Novel Dominant Mutation in the SOX10 Gene in a Chinese Family With Waardenburg Syndrome Type�II
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Doyne Honeycomb Retinal Dystrophy/Malattia Leventinese Induced by EFEMP1 Mutation in a Chinese Family
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Phenotype‐genotype Correlation of p.R124S Mutation in Granular Type 1 Corneal Dystrophy of Tunisian Origin
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a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
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Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome
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A Novel Mutation of GARS in a Chinese Family With Distal Hereditary Motor Neuropathy Type V
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