Pike MG

Title : Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters - Harrison_2011_Am.J.Med.Genet.A_155A_2826

Author(s) : Harrison V , Connell L , Hayesmoore J , McParland J , Pike MG , Blair E

Ref : American Journal of Medicine Genet A , 155A :2826 , 2011

Abstract :

PubMedSearch : Harrison_2011_Am.J.Med.Genet.A_155A_2826

PubMedID: 21964664

Title : Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies - Robb_2011_Neuromuscul.Disord_21_379

Author(s) : Robb SA , Sewry CA , Dowling JJ , Feng L , Cullup T , Lillis S , Abbs S , Lees MM , Laporte J , Manzur AY , Knight RK , Mills KR , Pike MG , Kress W , Beeson D , Jungbluth H , Pitt MC , Muntoni F

Ref : Neuromuscular Disorders , 21 :379 , 2011

Abstract :

PubMedSearch : Robb_2011_Neuromuscul.Disord_21_379

PubMedID: 21440438

Pike MG

References (2)

1. Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters - Harrison_2011_Am.J.Med.Genet.A_155A_2826

2. Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies - Robb_2011_Neuromuscul.Disord_21_379