Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 8 of 8 for "L-Alanine"
  1. Beta-ureidopropionase deficiency 
    ... carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to be released in the urine. Neurological problems ... acid and also breaks down N-carbamyl-beta-alanine to beta-alanine, ammonia, and carbon dioxide. Both ...
    https://medlineplus.gov/.../beta-ureidopropionase-deficiency - Genetics
  2. Primary hyperoxaluria 
    ... AGT deficiency Hyperoxaluria, primary Oxalosis Oxaluria, primary Peroxisomal alanine:glyoxylate aminotransferase deficiency Primary oxalosis Primary oxaluria Genetic ...
    https://medlineplus.gov/genetics/condition/primary-hyperoxaluria - Genetics
  3. Oculopharyngeal muscular dystrophy 
    ... copies of the protein building block (amino acid) alanine occur in a row. This stretch of alanines is known as a polyalanine tract. The role ... polyalanine tract that includes between 11 and 18 alanines. Typically, affected individuals with shorter polyalanine tracts tend ...
    https://medlineplus.gov/.../oculopharyngeal-muscular-dystrophy - Genetics
  4. Partington syndrome 
    ... where a protein building block (amino acid) called alanine is repeated multiple times. These stretches of alanines are known as polyalanine tracts. The most common ...
    https://medlineplus.gov/genetics/condition/partington-syndrome - Genetics
  5. Dihydropyrimidinase deficiency 
    ... produces molecules called beta-aminoisobutyric acid and beta-alanine. Both of these molecules are thought to protect ... Reduced production of beta-aminoisobutyric acid and beta-alanine may impair the function of these molecules in ...
    https://medlineplus.gov/.../condition/dihydropyrimidinase-deficiency - Genetics
  6. Familial paroxysmal nonkinesigenic dyskinesia 
    ... Fink J, Bird TD, Raskind WH. Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in ...
    https://medlineplus.gov/...lial-paroxysmal-nonkinesigenic-dyskinesia - Genetics
  7. GABA-transaminase deficiency 
    ... so this neurotransmitter and another molecule called beta-alanine accumulate abnormally in brain cells. This accumulation alters ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  8. Amish lethal microcephaly 
    ... in which the protein building block (amino acid) alanine is substituted for the amino acid glycine at ...
    https://medlineplus.gov/genetics/condition/amish-lethal-microcephaly - Genetics