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Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotype. [electronic resource] by
- Auer-Grumbach, Michaela
- Bode, Heiko
- Pieber, Thomas R
- Schabhüttl, Maria
- Fischer, Dirk
- Seidl, Rainer
- Graf, Elisabeth
- Wieland, Thomas
- Schuh, Reinhard
- Vacariu, Gerda
- Grill, Franz
- Timmerman, Vincent
- Strom, Tim M
- Hornemann, Thorsten
Producer: 20140102
In:
European journal of medical genetics vol. 56
Availability: No items available.
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