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UnknownSevere Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency.
Not available
S-EPMC5110450 | biostudies-literature
UnknownIdentifying recruitment strategies to improve the reach of evidence-based health promotion, disease prevention, and disease self-management interventions: a scoping review.
Not available
S-EPMC12023269 | biostudies-literature
UnknownCUL1 variants cause severe neurodevelopmental disorders: Insights from human genetics and a zebrafish model of microcephaly.
Not available
S-EPMC12704061 | biostudies-literature
UnknownDecrease of SYNGAP1 in GABAergic cells impairs inhibitory synapse connectivity, synaptic inhibition and cognitive function.
Not available
S-EPMC5105197 | biostudies-literature
UnknownA dual-color PAX7 and MYF5 in vivo reporter to investigate muscle stem cell heterogeneity in regeneration and aging.
Not available
S-EPMC11252486 | biostudies-literature
UnknownMutations in C5ORF42 cause Joubert syndrome in the French Canadian population.
Not available
S-EPMC3322222 | biostudies-literature
UnknownMutations in SYNGAP1 in autosomal nonsyndromic mental retardation.
Not available
S-EPMC2925262 | biostudies-literature
UnknownTruncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia.
Not available
S-EPMC3204930 | biostudies-literature
UnknownMutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.
Not available
S-EPMC2896783 | biostudies-literature
UnknownNicotinamide and pyridoxine stimulate muscle stem cell expansion and enhance regenerative capacity during aging.
Not available
S-EPMC11645154 | biostudies-literature
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