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 |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=179789687&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 179789687 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 17501172 38NP jtl: Orphanet Journal of Rare Diseases issn: 17501172 maglogo: N pubinfo: dt: 9/20/2024 vid: 19 iid: 1 pid: 24147 pub: BioMed Central artinfo: ui: 179789687 10.1186/s13023-024-03348-x 179789687 ppf: 1 ppct: 12 formats: tig: atl: A rare transcript homozygous variants in CLRN1(USH3A) causes Usher syndrome type 3 in a Chinese family. aug: au: Wang, Suyang Xu, Chen Yang Zhu, Yiming Ding, Wenjuan Hu, Jieyu Xu, Baicheng Guo, Yufen Liu, Xiaowen affil: https://ror.org/02erhaz63 Department of Otolaryngology-Head and Neck Surgery, Lanzhou University Second Hospital, No. 82 Cuiyingmen, 730030, Lanzhou, Gansu, PR China sug: pubtype: Academic Journal doctype: Journal Article ougenre: Article ab: language: English refInfo: holdings: @attributes: islocal: N |
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