Screen for MAOA Mutations in Target Human Groups

Brunner et al. [1993: Am J Hum Genet 52: 1032–1039–1993: Science 262:578–580] described males with an MAO-A deficiency state resulting from a premature stop codon in the coding region of the MAOA gene. This deficiency state was associated with abnormal levels of amines and amine metabolites in urine...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Am J Med Genet
Prif Awduron: Schuback, Deborah E., Mulligan, Evan L., Sims, Katherine B., Tivol, Elizabeth A., Greenberg, Benjamin D., Chang, Shu-Fen, Yang, Show-Lin, Mau, Yi-Chien, Shen, Chen-Yang, Ho, Mei-Shang, Yang, Nan-Hua, Butler, Merlin G., Fink, Stephen, Schwartz, Charles E., Berlin, F., Breakefield, Xandra O., Murphy, Dennis L., Hsu, Yun-Pung Paul
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 1999
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5253238/
https://ncbi.nlm.nih.gov/pubmed/10050962
Tagiau: Ychwanegu Tag
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