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Novel missense mutation in the RSPO4 gene in congenital hyponychia and evidence for a polymorphic initiation codon (p.M1I).
Khan, Tahir Naeem; Klar, Joakim; Nawaz, Sadia; Jameel, Muhammad; Tariq, Muhammad; Malik, Naveed Altaf; Baig, Shahid M; Dahl, Niklas.
Affiliation
  • Khan TN; Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechnology and Genetic Engineering (NIBGE), Faisalabad 38000, Pakistan.
BMC Med Genet ; 13: 120, 2012 Dec 13.
Article in En | MEDLINE | ID: mdl-23234511
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombospondins / Mutation, Missense / Nails, Malformed Type of study: Observational_studies / Prognostic_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2012 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombospondins / Mutation, Missense / Nails, Malformed Type of study: Observational_studies / Prognostic_studies Limits: Humans Country/Region as subject: Asia Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2012 Document type: Article Affiliation country: Country of publication: