Additional file 1 of Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness

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Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.29874468
Primary Topic
Genomics and Rare Diseases
Type
article
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article

Additional file 1 of Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness

Figshare
Genomics and Rare Diseases
article

Additional file 1 of Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness

article en

Abstract

No abstract available for this paper.
Figshare
Alfaisal University (SA), King Faisal Specialist Hospital & Research Centre (SA), King Saud University (SA), King Salman Center for Disability Research (SA)
Openalex Percentile: Top 55%
Genomics and Rare Diseases
DOIOpen Access PDFOpenAlex
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Additional file 1 of Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness · Figshare (2025) | TGRS Research Map | TGRS