Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Shahid Y. Khan
Correction: Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts
PLoS ONE
Multidisciplinary
Related publications
Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts
American Journal of Human Genetics
Genetics
Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus
Journal of Medical Genetics
Genetics
INPP5K Variant Causes Autosomal Recessive Congenital Cataract in a Pakistani Family
Clinical Genetics
Genetics
Autosomal Recessive Palmoplantar Keratoderma and Congenital Alopecia
Autosomal Recessive Severe Congenital Neutropenia Due to G6PC3 Deficiency
NIPAL4 Deletion Identified in an American Bully With Autosomal Recessive Congenital Ichthyosis and Response to Topical Therapy
Veterinary Medicine and Science
Veterinary
Functional Study ofTGM1missense Mutations in Autosomal Recessive Congenital Ichthyosis
Experimental Dermatology
Biochemistry
Dermatology
Molecular Biology
A Splice Mutation in a Syrian Autosomal Recessive Hypercholesterolemia Family Causes a Two-Nucleotide Deletion of mRNA
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency
