Three new mutations in the gene for the growth hormone (GH)-releasing hormone receptor in familial isolated GH deficiency type IB

Medicine & Life Sciences

• Type IB Isolated Growth Hormone Deficiency 100%
• somatotropin releasing hormone receptor 74%
• Pituitary Dwarfism 44%
• Mutation 25%
• Genes 18%
• Codon 14%
• Growth Hormone 14%
• Missense Mutation 10%
• Exons 8%
• CHO Cells 5%
• Histidine 5%
• Phenylalanine 5%
• Heterozygote 5%
• Leucine 5%
• Alanine 5%
• Introns 4%
• Cysteine 4%
• Siblings 4%
• Glutamic Acid 4%
• Phenotype 3%
• Serum 2%
• Therapeutics 1%

Chemical Compounds

• Growth Hormone 58%
• Mutation 38%
• Glutamic Acid 4%
• Leucine 4%
• Phenylalanine 4%
• Alanine 4%
• Histidine 4%
• Cysteine 3%