Sara E. Mole

Spectrum of mutations in the Batten disease gene, CLN3.

T. Lerner, P. Munroe, P. Taschner, 1997, American journal of human genetics.

Rapid diagnostic test for the major mutation underlying Batten disease.

P. Munroe, A. Syvänen, I. Järvelä, 1996, Journal of medical genetics.

Prenatal diagnosis of Batten's disease

P. Munroe, I. Järvelä, J. Rapola, 1996, The Lancet.

Workshop on the genetic and molecular basis of the neuronal ceroid lipofuscinoses. London, UK, 13-16 November 1997. Report and abstracts.

H. Goebel, S. Mole, R. Gardiner, 1998, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits.

P. Munroe, F. Andermann, Y. Crow, 1998, Human molecular genetics.

Genomic structure of three CLN3-like genes in Caenorhabditis elegans.

P. Kuwabara, S. Mole, W. Mitchell, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

A multiple interval physical map of the pericentromeric region of human chromosome 10

G. Finocchiaro, M. Jackson, L. Mulligan, 1994, Human Genetics.

A model for Batten disease protein CLN3: Functional implications from homology and mutations

R. W. Janes, P. Munroe, B. Wallace, 1996, FEBS letters.

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.

R. Norum, D. Easton, L. Mulligan, 1993, Human molecular genetics.

Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8.

A. Lehesjoki, S. Mole, W. Mitchell, 2001, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Epitope mapping.

S. Mole, S E Mole, Sara E. Mole, 1992, Methods in molecular biology.

Prevention of photoreceptor cell loss in a Cln6 mouse model of Batten disease requires CLN6 gene transfer to bipolar cells

A. Georgiadis, Y. Durán, J. Hoke, 2018 .