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type 2 Rhizomelic chondrodysplasia punctata

Also Known As:
Rhizomelic chondrodysplasia punctata, type 2; Chondrodysplasia punctata, rhizomelic, due to DHAPAT deficiency; DHAPAT deficiency; Dihydroxyacetonephosphate acyltransferase deficiency; GNPAT deficiency; Glyceronephosphate acyltransferase deficiency; Human dihydroxyacetonephosphate acyltransferase deficiency; Peroxisomal dihydroxyacetonephosphate acyltransferase deficiency; Type 2 rhizomelic chondrodysplasia punctata
Networked: 4 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Wieland, Felix: 1 article (06/2012)
2. Brugger, Britta: 1 article (06/2012)
3. Brodde, Alexander: 1 article (06/2012)
4. Lehmann, Wolf D: 1 article (06/2012)
5. Teigler, Andre: 1 article (06/2012)
6. Just, Wilhelm W: 1 article (06/2012)
7. Berger, Johannes: 1 article (06/2012)
8. Berdeaux, Olivier: 1 article (04/2012)
9. Acar, Niyazi: 1 article (04/2012)
10. Destaillats, Frédéric: 1 article (04/2012)

Related Diseases

1. Peroxisomal Disorders (Peroxisomal Disorder)
2. Rhizomelic Chondrodysplasia Punctata
3. Open-Angle Glaucoma (Glaucoma, Open Angle)

Related Drugs and Biologics

1. Ethyl Ether (Ether)