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A Ohtake

Showing results (61-70 of 65) with videos related to

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Journal of Medical Genetics|October 7, 2004
Mutations of the mitochondrial ND1 gene as a cause of MELASD M Kirby, R McFarland, A Ohtake, et al.
American Journal of Human Genetics|March 7, 2001
A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in AsiansY Okano, M Asada, A Fujimoto, et al.
Biochimica Et Biophysica Acta|January 28, 2014
Diagnosis and molecular basis of mitochondrial respiratory chain disorders: exome sequencing for disease gene identificationA Ohtake, K Murayama, M Mori, et al.
Clinical Genetics|June 16, 2016
DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burstK Zaha, H Matsumoto, M Itoh, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 17, 2017
Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetesM Okuno, T Ayabe, I Yokota, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Journal of Medical Genetics|October 7, 2004
Mutations of the mitochondrial ND1 gene as a cause of MELASD M Kirby, R McFarland, A Ohtake, et al.
American Journal of Human Genetics|March 7, 2001
A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in AsiansY Okano, M Asada, A Fujimoto, et al.
Biochimica Et Biophysica Acta|January 28, 2014
Diagnosis and molecular basis of mitochondrial respiratory chain disorders: exome sequencing for disease gene identificationA Ohtake, K Murayama, M Mori, et al.
Clinical Genetics|June 16, 2016
DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burstK Zaha, H Matsumoto, M Itoh, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 17, 2017
Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetesM Okuno, T Ayabe, I Yokota, et al.
Pageof 7