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 |