Work

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

Year: 2025

Type: article

Abstract: Additional file 1.

Source: Figshare

DOI: 10.6084/m9.figshare.29874468

Authors: AlQudairy, Hanan, AlMuhaizea, Mohammad A., Tohary, Mohamed, Alfuraih, Maissa, Alnafisah, Aisha, AlHargan, Aljouhra, Albader, Anoud, Jaber, Hadeel, Almass, Rawan, Albakheet, Albandary, Alsheddi, Terfa, AlObeid, Eman, Alrasheed, Maha M., Al-Odaib, Ali, AlZaidan, Hamad, AlSayed, Moeenaldeen D., Kaya, Namik

Institutions: King Faisal Specialist Hospital & Research Centre, Alfaisal University, King Saud University, King Salman Center for Disability Research

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W6902241907

FWCI:

Cites:

Cited by:

Related to: