NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.

M. Castori; E. M. Valente; M. A. Donati; S. Salvi; E. Fazzi; E. Procopio; T. Galluccio; F. Emma; B. Dallapiccola; E. Bertini

NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.

M. Castori, E. M. Valente, M. A. Donati, S. Salvi, E. Fazzi, E. Procopio, T. Galluccio, F. Emma, B. Dallapiccola, E. Bertini

Research output: Contribution to journal › Article › peer-review

Original language	English
Journal	Journal of Medical Genetics
Volume	42
Issue number	2
Publication status	Published - Feb 2005

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Cite this

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title = "NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.",

author = "M. Castori and Valente, {E. M.} and Donati, {M. A.} and S. Salvi and E. Fazzi and E. Procopio and T. Galluccio and F. Emma and B. Dallapiccola and E. Bertini",

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AU - Castori, M.

AU - Valente, E. M.

AU - Donati, M. A.

AU - Salvi, S.

AU - Fazzi, E.

AU - Procopio, E.

AU - Galluccio, T.

AU - Emma, F.

AU - Dallapiccola, B.

AU - Bertini, E.

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JO - Journal of Medical Genetics

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NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders.

ASJC Scopus subject areas

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