A novel mutation (S558X) causing choroideremia

التفاصيل البيبلوغرافية
العنوان: A novel mutation (S558X) causing choroideremia
المؤلفون: L. Beaufrere, Jacques Demaille, Mireille Claustres, Sylvie Tuffery, Christian P. Hamel, B. Arnaud
المصدر: Human Mutation. 8:395-395
بيانات النشر: Hindawi Limited, 1996.
سنة النشر: 1996
مصطلحات موضوعية: X Chromosome, Protein Prenylation, Biology, Polymerase Chain Reaction, Choroideremia, law.invention, chemistry.chemical_compound, law, Genetics, medicine, Humans, Point Mutation, Family, Genetics (clinical), Polymerase chain reaction, X chromosome, Adaptor Proteins, Signal Transducing, Alkyl and Aryl Transferases, Point mutation, DNA, Rab GTP-Binding Proteins, medicine.disease, Molecular biology, chemistry, rab GTP-Binding Proteins, Protein prenylation, Carrier Proteins, Novel mutation
تدمد: 1098-1004
1059-7794
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd8f5371a40f84e5d08d707eee0b2437Test
https://doi.org/10.1002/humu.1380080405Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....bd8f5371a40f84e5d08d707eee0b2437
قاعدة البيانات: OpenAIRE