X‐Linked Intellectual Developmental Disorder‐93 Caused by BRWD3 Mutation in Females: A Case Report and Literature Review
ABSTRACT Objective To report the clinical manifestations and genetic diagnosis of a female patient with X‐linked intellectual developmental disorder‐93 (XLID93, OMIM#300659) caused by a BRWD3 gene mutation. Systematically summarize the clinical and genetic characteristics of reported female cases an...
Shranjeno v:
| Principais autores: | , , , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Wiley
2026-06-01
|
| Serija: | Molecular Genetics & Genomic Medicine |
| Teme: | |
| Online dostop: | https://doi.org/10.1002/mgg3.70251 |
| Oznake: |
Brez oznak, prvi označite!
|
