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Results 1 - 10 of 138 for Cp
  1. CP gene 
    The CP gene provides instructions for making a protein called ceruloplasmin. Ceruloplasmin helps move iron from the organs and ...
    https://medlineplus.gov/genetics/gene/cp - Genetics
  2. ADAMTS13 gene 
    ... Willebrand factor-cleaving protease vWF-cleaving protease vWF-CP VWFCP Tests of ADAMTS13 PubMed A DISINTEGRIN-LIKE ...
    https://medlineplus.gov/genetics/gene/adamts13 - Genetics
  3. Hereditary pancreatitis 
    Hereditary pancreatitis is a genetic condition characterized by recurrent episodes of inflammation of the pancreas (pancreatitis). The pancreas produces enzymes ...
    https://medlineplus.gov/genetics/condition/hereditary-pancreatitis - Genetics
  4. Aceruloplasminemia 
    ... in this population are affected. Mutations in the CP gene cause aceruloplasminemia. The CP gene provides instructions for making a protein called ... to red blood cells to help carry oxygen.CP gene mutations result in the production of ceruloplasmin ...
    https://medlineplus.gov/genetics/condition/aceruloplasminemia - Genetics
  5. KRAS gene 
    ... Merbitz-Zahradnik T, Dvorsky R, Cirstea IC, Kratz CP, Zenker M, Wittinghofer A, Ahmadian MR. Germline KRAS ... S, Bollag G, Lyubynska N, Nguyen H, Kratz CP, Zenker M, Niemeyer CM, Molven A, Shannon K. ...
    https://medlineplus.gov/genetics/gene/kras - Genetics
  6. GBA gene 
    ... E, Bird TD, Leverenz JB, Tsuang D, Zabetian CP. Glucocerebrosidase gene mutations: a risk factor for Lewy ... S, Wittstock M, Wolfsberg TG, Wu YR, Zabetian CP, Zhao Y, Ziegler SG. Multicenter analysis of glucocerebrosidase ...
    https://medlineplus.gov/genetics/gene/gba - Genetics
  7. Optic atrophy type 1 
    ... ATROPHY 1; OPA1 PubMed Delettre-Cribaillet C, Hamel CP, Lenaers G. Optic Atrophy Type 1. 2007 Jul ... X, Charlin JF, Kaplan J, Odent S, Hamel CP, Procaccio V, Reynier P, Amati-Bonneau P. Molecular ...
    https://medlineplus.gov/genetics/condition/optic-atrophy-type-1 - Genetics
  8. Birt-Hogg-Dubé syndrome 
    ... ML, Duray P, Merino M, Choyke P, Pavlovich CP, Sharma N, Walther M, Munroe D, Hill R, ... 6108(02)00104-6. Citation on PubMed Pavlovich CP, Walther MM, Eyler RA, Hewitt SM, Zbar B, ...
    https://medlineplus.gov/genetics/condition/birt-hogg-dube-syndrome - Genetics
  9. Kidney stones 
    ... A, Miller NL, Monga M, Murad MH, Nelson CP, Pace KT, Pais VM Jr, Pearle MS, Preminger ... A, Miller NL, Monga M, Murad MH, Nelson CP, Pace KT, Pais VM Jr, Pearle MS, Preminger ...
    https://medlineplus.gov/genetics/condition/kidney-stones - Genetics
  10. Autosomal recessive congenital stationary night blindness 
    ... Moskova-Doumanova V, Berger W, Wissinger B, Hamel CP, Schorderet DF, De Baere E, Sharon D, Banin ... Defoort-Dhellemmes S, Wissinger B, Leveillard T, Hamel CP, Schorderet DF, De Baere E, Berger W, Jacobson ...
    https://medlineplus.gov/...ive-congenital-stationary-night-blindness - Genetics
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