Publication
| Kim S, Westphal V, Srikrishna G, Mehta DP, Peterson S, Filiano J, Karnes PS, Patterson MC, Freeze HH, Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie) The Journal of clinical investigation105:191-8 2000 |
| PubMed ID: 10642597 |
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| Records Return:
(1)
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| Catalog ID | Gender | Description | Collection_Type_id |
| GM20944 | Female | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie | GM |
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