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Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie

Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Cardiomyopathy, Familial Hypertrophic, 17 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

AGK regulates the progression to NASH by affecting mitochondria complex I function
AGK regulates the progression to NASH by affecting mitochondria complex I function

Frontiers | Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene
Frontiers | Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene

Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease
Genes | Free Full-Text | Molecular Insights into Mitochondrial Protein Translocation and Human Disease

Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library
Mitochondrial disease in children - Rahman - 2020 - Journal of Internal Medicine - Wiley Online Library

Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria

What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?
What is AGK Gene Sengers syndrome NGS Genetic DNA Test ?

Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar

Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press
Sengers syndrome in Asian Indians – two novel mutations and variant phenotype-genotype correlation - IOS Press

Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations - ScienceDirect
Mitochondrial citrate synthase crystals: Novel finding in Sengers syndrome caused by acylglycerol kinase (AGK) mutations - ScienceDirect

Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome
Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome

Sengers Syndrome: A Rare Cause of HOCM
Sengers Syndrome: A Rare Cause of HOCM

Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria - ScienceDirect

IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome
IJMS | Free Full-Text | Characterization of a Novel Splicing Variant in Acylglycerol Kinase (AGK) Associated with Fatal Sengers Syndrome

Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute
Media Release: Discovery-driven research leads to breakthrough in understanding rare Sengers syndrome | Bio21 Molecular Science & Biotechnology Institute

Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie

INBORN ERRORS OF METABOLISM
INBORN ERRORS OF METABOLISM

Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar
Acylglycerol Kinase Mutated in Sengers Syndrome Is a Subunit of the TIM22 Protein Translocase in Mitochondria. | Semantic Scholar

Mitochondrial diseases | Nature Reviews Disease Primers
Mitochondrial diseases | Nature Reviews Disease Primers

Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome. - Abstract - Europe PMC
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome. - Abstract - Europe PMC

Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life
Acylglycerol kinase: mitochondrial protein transport meets lipid biosynthesis | 2017 | Publications Archive | Publications | From analysis to synthesis - spanning all domains of life

Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients | Orphanet Journal of Rare Diseases | Full Text
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients | Orphanet Journal of Rare Diseases | Full Text

Sengers syndrome (Concept Id: C1859317)
Sengers syndrome (Concept Id: C1859317)

Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie
Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patie