Statistics

Total Visits

Views
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1 759

Total Visits per Month

November 2025 December 2025 January 2026 February 2026 March 2026 April 2026 May 2026
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1 17 19 15 18 32 29 16

File Downloads

Views
Enlace a_Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis.htm 357
Clinical Exome Sequencing Enables Congenital Sialidosis.pdf 339

Top Country Views

Views

Top City Views

Views