Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease

A. Weinhäusel,; I. Gomez Segovia,; A. Behmel,; P. Lind,; O.A. Haas,

doi:10.1515/IJDHD.2002.3.1.33

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Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease

A. Weinhäusel, , I. Gomez Segovia, , A. Behmel, , P. Lind, and O.A. Haas,

Published/Copyright: January 1, 2002

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From the journal International Journal on Disability and Human Development Volume 3 Issue 1

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Harvard
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Vancouver

Weinhäusel,, A., Segovia,, I. Gomez, Behmel,, A., Lind,, P. and Haas,, O.A.. "Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease" International Journal on Disability and Human Development, vol. 3, no. 1, pp. 33-36. https://doi.org/10.1515/IJDHD.2002.3.1.33

Weinhäusel,, A., Segovia,, I., Behmel,, A., Lind,, P. & Haas,, O. (). Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease. International Journal on Disability and Human Development, 3(1), 33-36. https://doi.org/10.1515/IJDHD.2002.3.1.33

Weinhäusel,, A., Segovia,, I., Behmel,, A., Lind,, P. and Haas,, O. () Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease. International Journal on Disability and Human Development, Vol. 3 (Issue 1), pp. 33-36. https://doi.org/10.1515/IJDHD.2002.3.1.33

Weinhäusel,, A., Segovia,, I. Gomez, Behmel,, A., Lind,, P. and Haas,, O.A.. "Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease" International Journal on Disability and Human Development 3, no. 1 (): 33-36. https://doi.org/10.1515/IJDHD.2002.3.1.33

Weinhäusel, A, Segovia, I, Behmel, A, Lind, P, Haas, O. Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease. International Journal on Disability and Human Development. ;3(1): 33-36. https://doi.org/10.1515/IJDHD.2002.3.1.33

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Articles in the same Issue

CONTENTS
Letter from the Editors
One SHOX Can Make You Short
Mutational Analysis of the Wolfram Syndrome Gene (WFS1) in Greek and Dominican Patients
Analysis of Components of the Growth Hormone (GH) Axis in (GH Deficient) Patients with Silver-Russell Syndrome
Methylation of the Androgen Receptor Gene in Cryptorchid Boys
Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease
BOOK REVIEWS. CALENDAR

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https://doi.org/10.1515/IJDHD.2002.3.1.33

Articles in the same Issue

CONTENTS
Letter from the Editors
One SHOX Can Make You Short
Mutational Analysis of the Wolfram Syndrome Gene (WFS1) in Greek and Dominican Patients
Analysis of Components of the Growth Hormone (GH) Axis in (GH Deficient) Patients with Silver-Russell Syndrome
Methylation of the Androgen Receptor Gene in Cryptorchid Boys
Identification of a Novel PRKARIA Mutation Predisposing for Carney Complex Disease
BOOK REVIEWS. CALENDAR