A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome. (Q51917869)
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scientific article published in May 2006
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome. |
scientific article published in May 2006 |
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A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome. (English)
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Hershkovitz T
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Hassoun G
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Indelman M
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Shlush LI
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Bergman R
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Pollack S
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Sprecher E
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1 May 2006
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31
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435-440
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