Results
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67201.
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TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease. [electronic resource] by
- Rayaprolu, Sruti
- Mullen, Bianca
- Baker, Matt
- Lynch, Timothy
- Finger, Elizabeth
- Seeley, William W
- Hatanpaa, Kimmo J
- Lomen-Hoerth, Catherine
- Kertesz, Andrew
- Bigio, Eileen H
- Lippa, Carol
- Josephs, Keith A
- Knopman, David S
- White, Charles L
- Caselli, Richard
- Mackenzie, Ian R
- Miller, Bruce L
- Boczarska-Jedynak, Magdalena
- Opala, Grzegorz
- Krygowska-Wajs, Anna
- Barcikowska, Maria
- Younkin, Steven G
- Petersen, Ronald C
- Ertekin-Taner, Nilüfer
- Uitti, Ryan J
- Meschia, James F
- Boylan, Kevin B
- Boeve, Bradley F
- Graff-Radford, Neill R
- Wszolek, Zbigniew K
- Dickson, Dennis W
- Rademakers, Rosa
- Ross, Owen A
Producer: 20130920
In:
Molecular neurodegeneration vol. 8
Availability: No items available.
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67202.
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67203.
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67204.
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Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy. [electronic resource] by
- Esposito, Teresa
- Sampaolo, Simone
- Limongelli, Giuseppe
- Varone, Antonio
- Formicola, Daniela
- Diodato, Daria
- Farina, Olimpia
- Napolitano, Filomena
- Pacileo, Giuseppe
- Gianfrancesco, Fernando
- Di Iorio, Giuseppe
Producer: 20140102
In:
Orphanet journal of rare diseases vol. 8
Availability: No items available.
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67205.
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67206.
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67207.
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67208.
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67209.
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67210.
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67211.
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67212.
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67213.
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67214.
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67215.
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67216.
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67217.
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67218.
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67219.
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67220.
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