cytosine has been researched along with Bloch-Siemens Syndrome in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Familial incontinentia pigmenti (IP [MIM 308310]), or Bloch-Sulzberger syndrome, is an X-linked dominant and male-lethal disorder." | 1.31 | Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma). ( Aradhya, S; Courtois, G; Israël, A; Levy, M; Lewis, RA; Nelson, DL; Rajkovic, A, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Aradhya, S | 1 |
| Courtois, G | 1 |
| Rajkovic, A | 1 |
| Lewis, RA | 1 |
| Levy, M | 1 |
| Israël, A | 1 |
| Nelson, DL | 1 |
1 other study available for cytosine and Bloch-Siemens Syndrome
| Article | Year |
|---|---|
Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma).
Topics: Amino Acid Sequence; Base Sequence; Carrier Proteins; Chromosome Aberrations; Cytosine; Exons; Femal | 2001 |