Pontocerebellar hypoplasia type 6: A British case with PEHO-like features.

Six subtypes of autosomal recessive pontocerebellar hypoplasia (PCH) have been identified and the genetic basis of four of these (PCH1, PCH2, PCH4, and PCH6) is known. PCH6 is associated with cerebral atrophy and multiple but variable respiratory chain defects in muscle and has been reported in one...

詳細記述

書誌詳細
主要な著者: Rankin, J, Brown, R, Dobyns, W, Harington, J, Patel, J, Quinn, M, Brown, G
フォーマット: Journal article
言語:English
出版事項: 2010

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