S. Kraner

发表

Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by ε-AChR subunit truncating mutations

O. Steinlein, J. Sieb, S. Kraner, 2000, Human Genetics.

Immature end-plates and utrophin deficiency in congenital myasthenic syndrome caused by epsilon-AChR subunit truncating mutations.

O. Steinlein, J. Sieb, S. Kraner, 2000, Human genetics.

Escherichia coli-cloned CFTR loci relevant for human artificial chromosome therapy.

F. Ascenzioni, M. Amaral, A. Ramalho, 2010, Human gene therapy.

Congenital myasthenic syndrome of Brahman cattle in South Africa

O. Steinlein, P. Thompson, A. Guthrie, 2003, The Veterinary Record.

Factors influencing the efficiency of generating genetically engineered pigs by nuclear transfer: multi-factorial analysis of a large data set

E. Wolf, R. Zimmer, A. Schnieke, 2013, BMC Biotechnology.

Congenital myasthenia in Brahman calves caused by homozygosity for a CHRNE truncating mutation

O. Steinlein, P. Thompson, J. Sieb, 2002, Neurogenetics.

Congenital myasthenic syndromes.

O. Steinlein, J. Sieb, S. Kraner, 2002, Seminars in pediatric neurology.

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutation.

O. Steinlein, B. Schrank, S. Tzartos, 2000, Annals of Neurology.

Congenital myasthenic syndrome with episodic apnea in patients homozygous for a CHAT missense mutation.

O. Steinlein, H. Strassburg, I. Laufenberg, 2003, Archives of neurology.

Severe congenital myasthenic syndrome due to homozygosity of the 1293insG ε‐acetylcholine receptor subunit mutation

O. Steinlein, B. Schrank, S. Tzartos, 2000 .

Congenital Myasthenic Syndrome in Cattle due to Homozygosity for a Truncating Mutation in the Acetylcholine Receptor (AChR) Epsilon‐Subunit Gene

O. Steinlein, P. Thompson, J. Sieb, 2003, Annals of the New York Academy of Sciences.