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UnknownPathway Anchored Multimodal Clustering Reveals Circuit Level Signatures in Parkinsons Disease.
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S-EPMC12724497 | biostudies-literature
UnknownLysosomal storage disorders identified in adult population from India: Experience of a tertiary genetic centre and review of literature.
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S-EPMC10910243 | biostudies-literature
UnknownDe novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India.
Not available
S-EPMC7616498 | biostudies-literature
UnknownDevelopment of national biobank for lysosomal storage disorders in India- a step towards advancing research and precision medicine.
Not available
S-EPMC12918591 | biostudies-literature
UnknownBurden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.
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S-EPMC11323464 | biostudies-literature
UnknownGenetic and allelic heterogeneity in 248 Indians with skeletal dysplasia.
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S-EPMC7617588 | biostudies-literature
UnknownClinical and genetic spectrum of 104 Indian families with central nervous system white matter abnormalities.
Not available
S-EPMC8918360 | biostudies-literature
UnknownDevelopment, validation and application of single molecule molecular inversion probe based novel integrated genetic screening method for 29 common lysosomal storage disorders in India.
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S-EPMC11088154 | biostudies-literature
UnknownAcute-on-chronic liver failure (ACLF): the 'Kyoto Consensus'-steps from Asia.
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S-EPMC11846769 | biostudies-literature
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