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UnknownRespiratory chain deficiency in nonmitochondrial disease.
Not available
S-EPMC4821083 | biostudies-literature
UnknownAllelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population.
Not available
S-EPMC2830196 | biostudies-literature
UnknownExploring the association between chorangioma and infantile haemangioma in singleton and multiple pregnancies: a case-control study in a Swedish tertiary centre.
Not available
S-EPMC5588969 | biostudies-literature
UnknownClinical heterogeneity of primary familial brain calcification due to a novel mutation in PDGFB.
Not available
S-EPMC4424129 | biostudies-literature
UnknownPhenotypic variability of TRPV4 related neuropathies.
Not available
S-EPMC4454778 | biostudies-literature
UnknownFrequency of rare recessive mutations in unexplained late onset cerebellar ataxia.
Not available
S-EPMC4539354 | biostudies-literature
UnknownBehr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene.
Not available
S-EPMC4568311 | biostudies-literature
UnknownIdentification of seven loci affecting mean telomere length and their association with disease.
Not available
S-EPMC4006270 | biostudies-literature
UnknownLonger genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk.
Not available
S-EPMC4767445 | biostudies-literature
UnknownVariants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.
Not available
S-EPMC4074274 | biostudies-literature
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