Mutations of the Gene Encoding the Protein Kinase A Type I-α Regulatory Subunit (PRKAR1A) in Patients with the “Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity, and Schwannomas” (Carney Complex)-Reference-Cited by-同舟云学术

Mutations of the Gene Encoding the Protein Kinase A Type I-α Regulatory Subunit (PRKAR1A) in Patients with the “Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity, and Schwannomas” (Carney Complex)

Published:2002-06 Issue:1 Volume:968 Page:3-21
ISSN:0077-8923
Container-title:Annals of the New York Academy of Sciences
language:en
Short-container-title:

Author:

STRATAKIS CONSTANTINE A.

Publisher

Wiley

Subject

History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.2002.tb04323.x/fullpdf

Reference24 articles.

1. Primary pigmented nodular adrenocortical disease and its associated conditions;Carney;Endocrinologist,1992

2. Carney complex: the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas;Carney;Semin. Dermatol.,1995

3. Carney complex: diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas;Stratakis;Am. J. Med. Genet.,1998

4. Dominant inheritance of the complex of myxomas, spotty pigmentation and endocrine overactivity;Carney;Mayo Clin. Proc.,1985

5. Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes;Stratakis;Front. Biosci.,2000

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