Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology-Reference-Cited by-同舟云学术

Biallelic mutations in huntington disease: A new case with just one affected parent, review of the literature and terminology

Author:

Uhlmann Wendy R.¹²,Peñaherrera Maria S.³⁴,Robinson Wendy P.³⁴,Milunsky Jeff M.⁵,Nicholson Jane M.¹⁶,Albin Roger L.⁷⁸

Affiliation:

1. Division of Molecular Medicine and Genetics; Department of Internal Medicine; University of Michigan; Ann Arbor Michigan

2. Department of Human Genetics; University of Michigan; Ann Arbor Michigan

3. Department of Medical Genetics; University of British Columbia; Vancouver British Columbia

4. Child and Family Research Institute; Vancouver British Columbia

5. Center for Human Genetics Inc.; Cambridge Massachusetts

6. Department of Obstetrics and Gynecology; University of Michigan; Ann Arbor Michigan

7. Department of Neurology; University of Michigan; Ann Arbor Michigan

8. VA Ann Arbor Healthcare System; Geriatrics Research, Education, and Clinical Center; Ann Arbor Michigan

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference55 articles.

2. ACMG/ASHG statement: laboratory guidelines for Huntington disease genetic testing;American College of Medical Genetics/American Society of Human Genetics Huntington Disease Genetic Testing Working Group;Am J Hum Genet,1998

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