Search

Search Constraints

You searched for: Author/Creator Jameel, Muhammad

Search Results

1. A 24‐generation‐old founder mutation impairs splicing of RBBP8 in Pakistani families affected with Jawad syndrome. Issue 4 (16th July 2021)

2. A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb‐girdle muscular dystrophy‐1 in three Pakistani pedigrees. Issue 2 (25th October 2021)

3. Mutations of KIF14 cause primary microcephaly by impairing cytokinesis. Issue 4 (14th October 2017)

4. Renal transplant from infant and neonatal donors is a feasible option for the treatment of end‐stage renal disease but is associated with increased early graft loss. Issue 11 (13th August 2018)

6. Whole exome sequencing identifies LRP1 as a pathogenic gene in autosomal recessive keratosis pilaris atrophicans. Issue 9 (3rd July 2015)