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Novel human pathological mutations. Gene symbol: GPR98. Disease: Usher syndrome 2C.
Hilgert, Nele.
Affiliation
  • Hilgert N; University of Antwerp, Wilrijk, Belgium. nele.hilgert@ua.ac.be
Hum Genet ; 125(3): 342, 2009 Apr.
Article in En | MEDLINE | ID: mdl-19320012
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Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Receptors, G-Protein-Coupled / Usher Syndromes Limits: Humans Language: En Journal: Hum Genet Year: 2009 Document type: Article Affiliation country:
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Sequence Deletion / Receptors, G-Protein-Coupled / Usher Syndromes Limits: Humans Language: En Journal: Hum Genet Year: 2009 Document type: Article Affiliation country: