Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T2 |
0-140 |
Sentence |
denotes |
We describe an ALG9-defective (congenital disorders of glycosylation type IL) patient who is homozygous for the p.Y286C (c.860A>G) mutation. |
T2 |
0-140 |
Sentence |
denotes |
We describe an ALG9-defective (congenital disorders of glycosylation type IL) patient who is homozygous for the p.Y286C (c.860A>G) mutation. |
T2 |
0-140 |
Sentence |
denotes |
We describe an ALG9-defective (congenital disorders of glycosylation type IL) patient who is homozygous for the p.Y286C (c.860A>G) mutation. |