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Q47618208-CFAF9D10-5EB9-415C-A46C-8253ADCD1A5C
Q47618208-CFAF9D10-5EB9-415C-A46C-8253ADCD1A5C
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http://www.wikidata.org/entity/statement/Q47618208-CFAF9D10-5EB9-415C-A46C-8253ADCD1A5C
Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.
P1433
Q47618208-CFAF9D10-5EB9-415C-A46C-8253ADCD1A5C
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Statement
http://www.wikidata.org/entity/statement/Q47618208-CFAF9D10-5EB9-415C-A46C-8253ADCD1A5C
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4d6d08978b016aa9c917fcda56b26637689988de
P1433
European Journal of Human Genetics