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Diabetes and deafness
Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G Heterogeneidade Fenotípica De Uma Família Causada
Identification of P.A684V Missense Mutation in the WFS1 Gene As a Frequent Cause of Autosomal Dominant Optic Atrophy and Hearing
Maternally Inherited Diabetes and Deafness (MIDD) Syndrome with M.3243A>G Mutation Associated with Renal Failure — a Case Report
The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes
Mitochondrial Diseases in North America an Analysis of the NAMDC Registry
Maternally Inherited Diabetes and Deafness Presenting with Ptosis and Macular Pattern Dystrophy Olufunmilola Ogun, Claire Sheldon and Jason J.S
Frequency and Clinical Features of Patients with Sensorineural Hearing Loss Associated with the A3243G Mutation of the Mitochondrial DNA in Otorhinolaryngic Clinics
Diabetes and Deafness; Not All MODY Is MELAS
Overview on Visceral Manifestations of Mitochondrial Disorders
The Effects of Coenzyme Q10 Treatment on Maternally Inherited Diabetes Mellitus and Deafness, and Mitochondrial DNA 3243 (A to G) Mutation
Molecular Bases of Hearing Loss in Multi-Systemic Mitochondrial
Identification of Novel Mutations of the WFS1 Gene in Brazilian Patients with Wolfram Syndrome
Met5. Mitochondrial Disorders.Pdf
Mitochondrial Syndromes Revisited
Mitochondrial Diabetes Molecular Mechanisms and Clinical Presentation J
Leigh Syndrome in a Pedigree Harboring the M.1555A>G Mutation
And Cell-Type–Specific Manifestations of Heteroplasmic Mtdna
Design, Development and Deployment of a Web-Based Interoperable Registry for Inherited Retinal Dystrophies in Portugal: the IRD
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Heterogeneous Phenotypic Manifestations of Maternally
MIDD Or Maternally Inherited Diabetes & Deafness
An Example of Monogenic Diabetes Mellitus
Mitochondria P F Chinnery, E a Schon
Mitochondrial Disease and Endocrine Dysfunction Jasmine Chow1
MT-TK Gene Mitochondrially Encoded Trna Lysine
Brief Genetics Report Defining the Importance of Mitochondrial Gene Defects in Maternally Inherited Diabetes by Sequencing the Entire Mitochondrial Genome Alan T.W
Mitochondrial Disorders and the Eye
Loss-Of-Function Mutation in Thiamine Transporter 1 in a Family with Autosomal Dominant Diabetes
Mitochondrial DNA
Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
Maternally Inherited Diabetes and Deafness and Mitochondrial Encephalopathy Lactic Acidosis and Stroke Like Episodes
Maternally Inherited Diabetes and Deafness
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MT-TL1 Gene Mitochondrially Encoded Trna Leucine 1 (UUA/G)