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Subba Rao Indugula

1PUBLICATIONS

0CO-AUTHORS

Neurogenetics

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Publications (1)

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|Feb 14, 2022

Exome sequencing identified a novel HIST1H1E heterozygous protein-truncating variant in a 6-month-old male patient with Rahman syndrome: A case report.

Subba Rao Indugula, Sofia Saenz Ayala, Francesco Vetrini

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