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Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency.

We have determined the mutation in a child with partial adenosine deaminase (ADA) deficiency who is phenotypically homozygous for a mutant ADA gene encoding a heat-labile enzyme (Am. J. Hum. Genet. 38: 13-25). Sequencing of cDNA demonstrated a C to A transversion that results in the replacement of a...

Бүрэн тодорхойлолт

-д хадгалсан:
Номзүйн дэлгэрэнгүй
-д хэвлэсэн:J Clin Invest
Үндсэн зохиолчид: Hirschhorn, R, Tzall, S, Ellenbogen, A, Orkin, S H
Формат: Artigo
Хэл сонгох:Inglês
Хэвлэсэн: American Society for Clinical Investigation 1989
Нөхцлүүд:
Онлайн хандалт:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC303706/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2783588/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113909
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