FAMILIAL AMYLOID POLYNEUROPATHIES
\famˈɪlɪəl ˈamɪlˌɔ͡ɪd pˌɒlɪnjuːɹˈɒpəθɪz], \famˈɪlɪəl ˈamɪlˌɔɪd pˌɒlɪnjuːɹˈɒpəθɪz], \f_a_m_ˈɪ_l_ɪ__ə_l ˈa_m_ɪ_l_ˌɔɪ_d p_ˌɒ_l_ɪ_n_j_uː_ɹ_ˈɒ_p_ə_θ_ɪ_z]\
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Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.
By DataStellar Co., Ltd
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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.-.
Nearby Words
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- Familial Amyloid Polyneuropathies
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- familial amyloidoses
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