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Article Dans Une Revue Human Mutation Année : 2021

The corrected breakpoint sequence of the homozygous SPINK1 deletion causing severe infantile isolated exocrine pancreatic insufficiency

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hal-03617789 , version 1 (23-03-2022)

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Emmanuelle Masson, Claude Férec, Jian-Min Chen. The corrected breakpoint sequence of the homozygous SPINK1 deletion causing severe infantile isolated exocrine pancreatic insufficiency. Human Mutation, 2021, 42 (2), pp.216-217. ⟨10.1002/humu.24153⟩. ⟨hal-03617789⟩
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