Results
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7181.
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7182.
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7183.
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7184.
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7185.
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7186.
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Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding. [electronic resource] by
- Wenzel, Katrin
- Carl, Miriam
- Perrot, Andreas
- Zabojszcza, Joanna
- Assadi, Maziar
- Ebeling, Martin
- Geier, Christian
- Robinson, Peter N
- Kress, Wolfram
- Osterziel, Karl-Josef
- Spuler, Simone
Producer: 20060626
In:
Human mutation vol. 27
Availability: No items available.
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7187.
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7188.
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7189.
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7190.
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7191.
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7192.
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7193.
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7194.
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7195.
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7196.
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7197.
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7198.
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7199.
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7200.
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A nonstop mutation in the factor (F)X gene of a severely haemorrhagic patient with complete absence of coagulation FX. [electronic resource] by
- Ameri, Afshin
- Machiah, Deepa K
- Tran, Thuy T
- Channell, Cynthia
- Crenshaw, Valerie
- Fernstrom, Karl
- Khachidze, Manana
- Duncan, Alexander
- Fuchs, Sebastien
- Howard, Tom E
Producer: 20080226
In:
Thrombosis and haemostasis vol. 98
Availability: No items available.
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