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...

Popoln opis

Bibliografske podrobnosti
Main Authors: Rankin, J, Brown, R, Dobyns, W, Harington, J, Patel, J, Quinn, M, Brown, G
Format: Journal article
Jezik:English
Izdano: 2010

Podobne knjige/članki