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Publications by Xinqian Geng
De Novo Mutation of M.3243A>G Together With M.16093T>C Associated With Atypical Clinical Features in a Pedigree With MIDD Syndrome
Journal of Diabetes Research
Endocrinology
Metabolism
Diabetes
Related publications
Glucose Metabolism Derangements in Adults With the MELAS M.3243A>G Mutation
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
Natural History of MELAS Associated With Mitochondrial DNA M.3243A>G Genotype
Neurology
Neurology
Fear of Disease Progression in Carriers of the M.3243A > G Mutation
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Authors' Reply to 'Heteroplasmy of the M.3243A>G Mutation May Influence Phenotypic Heterogeneity'
Internal Medicine
Internal Medicine
Medicine
Illness-Induced Exacerbation of Leigh Syndrome in a Patient With the MTATP6 Mutation, M. 9185 T>C
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report
Frontiers in Genetics
Genetics
Molecular Medicine
Aggressive Periodontitis Associated With Kindler Syndrome in a Large Kindler Syndrome Pedigree
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
A Novel De Novo Mutation in CEACAM16 Associated With Postlingual Hearing Impairment
Molecular Syndromology
Genetics
Reduced Bone Mineral Density in M.3243A > G Carriers May Be Multifactorial
Journal of Bone and Mineral Research
Endocrinology
Orthopedics
Sports Medicine
Metabolism
Diabetes