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Publications by Houfa Yin
Identification and Functional Analysis of a Novel MIP Gene Mutation Associated With Congenital Cataract in a Chinese Family
PLoS ONE
Multidisciplinary
Cytokine Profiling Reveals Increased Serum Inflammatory Cytokines in Idiopathic Choroidal Neovascularization
Related publications
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
Identification of a Novel Missense FBN2 Mutation in a Chinese Family With Congenital Contractural Arachnodactyly Using Exome Sequencing
PLoS ONE
Multidisciplinary
Identification of a Novel Frameshift Mutation in PITX2 Gene in a Chinese Family With Axenfeld-Rieger Syndrome
Journal of Zhejiang University: Science B
Genetics
Pharmacology
Molecular Biology
Biochemistry
Veterinary
Medicine
Toxicology
Pharmaceutics
Identification of a Novel TCOF1 Mutation in a Chinese Family With Treacher Collins Syndrome
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Identification of aCRYABMutation Associated With Autosomal Dominant Posterior Polar Cataract in a Chinese Family
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
A Novel FBN2 Mutation Cosegregates With Congenital Contractural Arachnodactyly in a Five-Generation Chinese Family
Clinical Case Reports
Medicine
A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly
Frontiers in Genetics
Genetics
Molecular Medicine
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family
Bioscience Reports
Biochemistry
Cell Biology
Molecular Biology
Biophysics