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J A Mayr

Showing results (11-20 of 15) with videos related to

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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 3, 2021
[Molecular medicine: pathobiochemistry as the key to personalized treatment of inherited diseases]J A Mayr, R G Feichtinger, M T Achleitner, et al.
Journal of Inherited Metabolic Disease|February 10, 2004
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex IS M S Budde, L P W J van den Heuvel, R J P Smeets, et al.
Journal of Inherited Metabolic Disease|July 10, 2009
Danon disease: case report and detection of new mutationG Regelsberger, R Höftberger, W F Pickl, et al.
Neuromuscular Disorders : NMD|October 21, 2006
Deficiency of mitochondrial ATP synthase of nuclear genetic originW Sperl, P Jesina, J Zeman, et al.
Journal of Inherited Metabolic Disease|November 20, 2009
PDH E1β deficiency with novel mutations in two patients with Leigh syndromeE Quintana, J A Mayr, M T García Silva, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 3, 2021
[Molecular medicine: pathobiochemistry as the key to personalized treatment of inherited diseases]J A Mayr, R G Feichtinger, M T Achleitner, et al.
Journal of Inherited Metabolic Disease|February 10, 2004
Clinical heterogeneity in patients with mutations in the NDUFS4 gene of mitochondrial complex IS M S Budde, L P W J van den Heuvel, R J P Smeets, et al.
Journal of Inherited Metabolic Disease|July 10, 2009
Danon disease: case report and detection of new mutationG Regelsberger, R Höftberger, W F Pickl, et al.
Neuromuscular Disorders : NMD|October 21, 2006
Deficiency of mitochondrial ATP synthase of nuclear genetic originW Sperl, P Jesina, J Zeman, et al.
Journal of Inherited Metabolic Disease|November 20, 2009
PDH E1β deficiency with novel mutations in two patients with Leigh syndromeE Quintana, J A Mayr, M T García Silva, et al.
Pageof 2