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Publications by Linxin Jiang
A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Related publications
A Recurring FBN1 Gene Mutation in Neonatal Marfan Syndrome
Archives of Pediatrics & Adolescent Medicine
a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family
G3: Genes, Genomes, Genetics
Medicine
Genetics
Molecular Biology
A Novel Heterozygous Mutation in Cardiac Calsequestrin Causes Autosomal Dominant Catecholaminergic Polymorphic Ventricular Tachycardia
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Homozygosity for a FBN1 Missense Mutation: Clinical and Molecular Evidence for Recessive Marfan Syndrome
European Journal of Human Genetics
Genetics
A Novel Mutation in the Connexin 46 Gene Causes Autosomal Dominant Congenital Cataract With Incomplete Penetrance
Journal of Medical Genetics
Genetics
Autosomal Dominant Diabetes Arising From a Wolfram Syndrome 1 Mutation
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
A Mutation in the Dimerization Domain of Filamin C Causes a Novel Type of Autosomal Dominant Myofibrillar Myopathy
American Journal of Human Genetics
Genetics
Autosomal Dominant Robinow Syndrome
An Autosomal Dominant Mutation in Calsequestrin 2 Causes CPVT Without Changing Protein Levels
Biophysical Journal
Biophysics
