INBORN AMINO ACIDOPATHY
\ˈɪnbɔːn ɐmˈiːnə͡ʊ ɐsɪdˈɒpəθɪ], \ˈɪnbɔːn ɐmˈiːnəʊ ɐsɪdˈɒpəθɪ], \ˈɪ_n_b_ɔː_n ɐ_m_ˈiː_n_əʊ ɐ_s_ɪ_d_ˈɒ_p_ə_θ_ɪ]\
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Disorders affecting amino acid metabolism. The majority of these disorders are inherited and present in the neonatal period with metabolic disturbances (e.g., ACIDOSIS) and neurologic manifestations. They are present at birth, although they may not become symptomatic until later in life.
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Proto Oncogene Proteins c erbB 2
- cell surface protein-tyrosine kinase that is found to be overexpressed in significant number adenocarcinomas. It has extensive homology can heterodimerize EGF EPIDERMAL GROWTH FACTOR), 3 receptor (RECEPTOR, 3) and the 4 receptor. Activation of erbB-2 receptor occurs during heterodimer formation with a ligand-bound erbB family members. EC 2.7.11.-.