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Glut1 deficiency and alternating hemiplegia of childhood.
Not available
S-EPMC2796456
|
biostudies-literature
Cite
Paroxysmal eye-head movements in Glut1 deficiency syndrome.
Not available
S-EPMC5405761
|
biostudies-literature
Cite
CoQ
10
Deficiency Is Not a Common Finding in GLUT1 Deficiency Syndrome.
Not available
S-EPMC5059199
|
biostudies-literature
Cite
Hypotonia-cystinuria 2p21 deletion syndrome: Intrafamilial variability of clinical expression.
Not available
S-EPMC8607452
|
biostudies-literature
Cite
Regulatory environment for novel therapeutic development in mitochondrial diseases.
Not available
S-EPMC9326497
|
biostudies-literature
Cite
Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants.
Not available
S-EPMC8157239
|
biostudies-literature
Cite
The North American mitochondrial disease registry.
Not available
S-EPMC7323997
|
biostudies-literature
Cite
Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome.
Not available
S-EPMC10187726
|
biostudies-literature
Cite
Circulating markers of NADH-reductive stress correlate with mitochondrial disease severity.
Not available
S-EPMC7810486
|
biostudies-literature
Cite
Deoxynucleoside Therapy for Thymidine Kinase 2-Deficient Myopathy.
Not available
S-EPMC7586249
|
biostudies-literature
Cite
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