Disease #00031 (PBP (Progressive Bulbar Palsy))

Official abbreviation PBP
Name Progressive Bulbar Palsy
OMIM ID -
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease -
Associated with 2 genes SOD1, TTR
Associated tissues -
Disease features -
Remarks -


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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AscendingIndividual ID     

Reference     

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Genes screened

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Owner     
00003929 Ikeda K1, Kinoshita M, Takamiya K, Iwasaki Y, Tomita Y, Nakano I I, Nakazato M.(1998) - - PBP - TTR TTR 1 1 Y Yang
00003930 Nanri K1, Utsumi H, Yamada M, Takata Y, Matsumura A, Kougo K, Sekine S, Ogawa D, Toyoda M.(2002) - - PBP - TTR TTR 1 1 Y Yang
00003931 Ito K1, Uchiyama T, Fukutake T, Arai K, Kanesaka T, Hattori T.(2002) - - PBP - SOD1 SOD1 1 1 Y Yang
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