APPALACHIAN TYPE FAMILIAL AMYLOID POLYNEUROPATHY
\ɐpɐlˈe͡ɪʃən tˈa͡ɪp famˈɪlɪəl ˈamɪlˌɔ͡ɪd pˌɒlɪnjuːɹˈɒpəθɪ], \ɐpɐlˈeɪʃən tˈaɪp famˈɪlɪəl ˈamɪlˌɔɪd pˌɒlɪnjuːɹˈɒpəθɪ], \ɐ_p_ɐ_l_ˈeɪ_ʃ_ə_n t_ˈaɪ_p 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]\
Definitions of APPALACHIAN TYPE FAMILIAL AMYLOID POLYNEUROPATHY
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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.
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bcr v abl Oncogene
- Retrovirus-associated DNA sequences (abl) originally isolated from Abelson murine leukemia virus (Ab-MuLV). proto-oncogene abl (codes for a protein that member tyrosine kinase family. human c-abl gene is located at 9q34.1 on the long arm of chromosome 9. It activated by translocation to bcr 22 in chronic myelogenous leukemia.