A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family.
| Publicado en: | Orphanet Journal of Rare Diseases Vol. 19; no. 1; pp. 1 - 13 |
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| Autores principales: | , , , , , , , |
| Formato: | Journal Article |
| Publicado: |
BioMed Central
9/20/2024
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| Acceso en línea: | Ver este registro en EBSCOhost |