Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A (Q24538812)
scientific article published on March 1, 1998
Language:
(P31) (Q13442814)
(P50) (Q87778355)
(Q28322538)
(P304) 542-550
(P407) (Q1860)
(P433) 3
(P478) 62
(P577) Sunday, March 1, 1998
Sunday, March 1, 1998
(P921) (Q49985)
(Q80726)
(P953) http://www.cell.com/article/S0002929707638348/pdf
https://europepmc.org/articles/PMC1376957
https://europepmc.org/articles/PMC1376957?pdf=render
https://api.elsevier.com/content/article/PII:S0002929707638348?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929707638348?httpAccept=text/plain
(P1433) (Q4744249)
(P1476) "Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1A" (language: en)
"Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A" (language: en)
(P2093) E. Schollen
J. J. Cassiman
J. Jaeken
(P2860) (Q24318956)
(Q24675799)
(Q28118150)
(Q28258535)
(Q28272713)
(Q28235485)
(Q28593471)
(Q33869809)
(Q33678333)
(Q34797675)
(Q34348805)
(Q33624870)
(Q34058550)
(Q48334324)
(Q45345362)
(Q67973815)
(Q70869007)
(Q60042765)
(Q71943546)
(Q73269162)
(Q60042760)
(Q63681437)
other details
description scientific article published on March 1, 1998

External Links