Academic Journal
LB1721 A novel pathogenic TPCN2 mutation detected for the first time in a Caucasian patient confirms the dominant inheritance of albinism
| العنوان: | LB1721 A novel pathogenic TPCN2 mutation detected for the first time in a Caucasian patient confirms the dominant inheritance of albinism |
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| المؤلفون: | Nagy, N., Pal, M., Kun, J., Bence, G., Urban, P., Medvecz, M., Fábos, B., Neller, A., Danis, J., Hammad, Z., AlMarsomy, S., Adam, E., Gyenesei, A., Szell, M. |
| المصدر: | Journal of Investigative Dermatology ; volume 143, issue 9, page B20 ; ISSN 0022-202X |
| بيانات النشر: | Elsevier BV |
| سنة النشر: | 2023 |
| المجموعة: | ScienceDirect (Elsevier - Open Access Articles via Crossref) |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1016/j.jid.2023.06.098 |
| الاتاحة: | http://dx.doi.org/10.1016/j.jid.2023.06.098 https://api.elsevier.com/content/article/PII:S0022202X23022431?httpAccept=text/xml https://api.elsevier.com/content/article/PII:S0022202X23022431?httpAccept=text/plain |
| Rights: | https://www.elsevier.com/tdm/userlicense/1.0/ |
| رقم الانضمام: | edsbas.E35509B |
| قاعدة البيانات: | BASE |
| DOI: | 10.1016/j.jid.2023.06.098 |
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