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WGA Rescources

Bouhouche A 1

Showing records 1 to 1 | Display all abstracts from Bouhouche A

9127 Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma
Azzedine H; Bolino A; Taieb T; Birouk N; Di Duca M; Bouhouche A; Benamou S; Mrabet A; Hammadouche T; Chkili T
American Journal of Human Genetics 2003; 72: 1141-1153

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