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Details on Person Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement
| Class:Id | LiteratureReference:2730945 |
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| _displayName | Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement |
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| _timestamp | 2012-12-05 14:16:16 |
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| author | [Person:2731007] Pangrazio, Alessandra
[Person:2730975] Poliani, Pietro Luigi
[Person:2730971] Megarbane, André
[Person:2730985] Lefranc, Gérard
[Person:2730955] Lanino, Edoardo
[Person:2730967] Di Rocco, Maja
[Person:2730990] Rucci, Francesca
[Person:2730982] Lucchini, Franco
[Person:2731016] Ravanini, Maria
[Person:2730942] Facchetti, Fabio
[Person:2731012] Abinun, Mario
[Person:2537572] Vezzoni, Paolo
[Person:2731019] Villa, Anna
[Person:2730979] Frattini, Annalisa |
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| created | [InstanceEdit:2730935] Jassal, Bijay, 2012-12-05 |
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| journal | J. Bone Miner. Res. |
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| pages | 1098-105 |
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| pubMedIdentifier | 16813530 |
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| title | Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement |
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| volume | 21 |
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| year | 2006 |
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| (literatureReference) | [Reaction:2730959] CLCN7:OSTM1 exchanges Cl- for H+ [Homo sapiens] |
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