TXNDC3/NME8 抗体
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Latest Publications for our TXNDC3/NME8 抗体
: "A common variant in combination with a nonsense mutation in a member of the thioredoxin family causes primary ciliary dyskinesia." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 104, Issue 9, pp. 3336-41, (2007) (PubMed).Aliases for TXNDC3/NME8 抗体
NME/NM23 family member 8 (NME8) 抗体NME/NM23 family member 8 (Nme8) 抗体
1700056P15Rik 抗体
CILD6 抗体
NM23-H8 抗体
sptrx-2 抗体
Sptrx-2 抗体
SPTRX2 抗体
Sptrx2 抗体
TXNDC3 抗体
Txndc3 抗体