Publication:
Spectrum of Phenotypic Findings in Individuals with Joubert Syndrome and Clinical Correlation with Identified Mutations in the NPHP1,AHI1, and RPGRIP1L Genes

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Abstract

Description

132nd Annual Meeting of the American-Neurological-Association -- OCT 07-10, 2007 -- Washington, DC

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Citation

WoS Q

Scopus Q

Source

Volume

62

Issue

5

Start Page

537

End Page

538

Endorsement

Review

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