Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene.
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Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene.
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Characterization of a Case of ...... us Mutations in the SGSH Gene.
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Characterization of a Case of ...... us Mutations in the SGSH Gene.
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type
label
Characterization of a Case of ...... us Mutations in the SGSH Gene.
@en
Characterization of a Case of ...... us Mutations in the SGSH Gene.
@nl
prefLabel
Characterization of a Case of ...... us Mutations in the SGSH Gene.
@en
Characterization of a Case of ...... us Mutations in the SGSH Gene.
@nl
P2093
P2860
P1433
P1476
Characterization of a Case of ...... ous Mutations in the SGSH Gene
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P2093
Jewell C Ward
Justin Wilkin
Kathryn W Byrd
Natalie C Kerr
P2860
P304
P356
10.3109/13816810.2015.1028647
P577
2015-09-02T00:00:00Z