Deficit di piruvato chinasi
- Author: B. Glader, W. Barcellini, R.Grace
- Yili: 2019
- Bo‘lim: O'QUV ADABIYOTLAR
- Ko‘rishlar: 12
- Fayl: Mavjud
Summary: The text provides structured guidance aimed at raising clinical awareness and improving the timely diagnosis of this genetic disease. It thoroughly covers the underlying molecular mechanisms, clinical signs ranging from severe neonatal jaundice to chronic fatigue, and various diagnostic pathways including enzymatic assays and genetic testing. Gematologiya.
- Kitob ID: 6383
- Format: PDF / Elektron kitob
- Yaratilgan sana: 2026-08-25 15:01:10
- Ko‘rishlar soni: 12
Kitob tavsifi
The text provides structured guidance aimed at raising clinical awareness and improving the timely diagnosis of this genetic disease. It thoroughly covers the underlying molecular mechanisms, clinical signs ranging from severe neonatal jaundice to chronic fatigue, and various diagnostic pathways including enzymatic assays and genetic testing.
Gematologiya.
| Maydon | Qiymat |
|---|---|
| ID | 6383 |
| Nomi | Deficit di piruvato chinasi |
| Muallif | B. Glader, W. Barcellini, R.Grace |
| Bo‘lim | O'QUV ADABIYOTLAR |
| Nashr yili | 2019 |
| Ko‘rishlar | 12 |
| Fayl hajmi | 5.37 MB |
| Yaratilgan sana | 2026-08-25 15:01:10 |
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