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Mutations in a novel gene Dymeclin (FLJ20071) are responsible for Dyggve–Melchior–Clausen syndrome
Hum. Mol. Genet.
El Ghouzzi et al. 12 (3): 357.
Supplementary Material
SBF2 Human cDNA
Files in this Data Supplement:
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Mutations in a novel gene Dymeclin (FLJ20071) are responsible for Dyggve–Melchior–Clausen syndrome
Hum. Mol. Genet.
El Ghouzzi et al. 12 (3): 357.
SBF2 Human cDNA
Files in this Data Supplement:
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