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GAL 1
- Galactose-1-phosphate uridyltransferase is a blood test that measures the level of a substance called GALT, which helps break down milk sugars in your body. A low level of this substance causes a condition called galactosemia .
- ... its normal activity. More About This Health Condition Gal-1-P uridylyltransferase Galactosephosphate Uridylyltransferase GALT_HUMAN UDP Galactose ...
- Citizen's Guide to Pest Control and Pesticide Safety (Environmental Protection Agency) - PDFPesticides/Start Here ... Pesticides ... Environmental Protection Agency ... PDF ... pesticide,citizen's guide,pest control,pesticide safety
- ... 3; CSNBAD3 NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1 PubMed Gal A, Orth U, Baehr W, Schwinger E, Rosenberg ... 2010;664:263-72. doi: 10.1007/978-1-4419-1399-9_30. Citation on PubMed ... HJ, Rosenberg T, Gal A. p.Gln200Glu, a putative constitutively active mutant ...
- About Alpha-gal Syndrome (Centers for Disease Control and Prevention)Food Allergy/Specifics ... Food Allergy ... Tick Bites/Specifics ... Tick Bites ... Centers for Disease Control and Prevention ... Alpha-gal syndrome can occur after certain types ...
- ... Bartsch O, von der Wense A, Meinecke P, Gal A. Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp. Cytogenet Genome Res. 2002;99(1-4):297-302. doi: 10.1159/000071607. Citation ...
- Food Allergy (American Academy of Allergy, Asthma, and Immunology)Food Allergy/Start Here ... Food Allergy ... American Academy of Allergy, Asthma, and Immunology ... AAAAI, the experts in allergy and immunology, provide an overview ...
- ... Finckh U, Schroder J, Ressler B, Veske A, Gal A. Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am J Med Genet. 2000 May 1;92(1):40-6. doi: 10.1002/(sici) ...
- ... Finckh U, Schroder J, Ressler B, Veske A, Gal A. Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. Am J Med Genet. 2000 May 1;92(1):40-6. doi: 10.1002/(sici) ...
- ... C-Salcedo Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat Genet. 2001 Jan;27(1):108-12. doi: 10.1038/83667. Citation on ...