Monoamine oxidase deficiency in males with an X chromosome deletion-Reference-Cited by-同舟云学术

Monoamine oxidase deficiency in males with an X chromosome deletion

Published:1989-01 Issue:1 Volume:2 Page:1069-1076
ISSN:0896-6273
Container-title:Neuron
language:en
Short-container-title:Neuron

Author:

Sims K.B.,de la Chapelle A.,Norio R.,Sankila E-M.,Hsu Y.-P.P,Rinehart W.B.,Corey T.J.,Ozelius L.,Powell J.F.,Bruns G.,Gusella J.F.,Murphy D.L.,Breakefield X.O.

Publisher

Elsevier BV

Subject

General Neuroscience

Reference84 articles.

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5. Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms;Breakefield;J. Neurogenet.,1986

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