درشن
مائے نی جہلم جاون دے
پیا نوں دکھ سناون دے
پیا بناں میں ریہہ نہ سکدی
ہر دم اوہدیاں راہواں تکدی
تک تک راہواں کدی ناں اکدی
دل دا شوق نبھاون دے
مائے نی جہلم جاون دے
مدتاں ہوئیاں ملن نہ ہویا
دل رہندا اے کھویا کھویا
اکھیاں ہنجواں ہار پرویا
اے مالا گل وچ پاون دے
مائے نی جہلم جاون دے
پہاڑ ٹلے دا نظریں آوے
جے کر سوہنا تلک لگاوے
گجھڑا روگ اندر دا جاوے
دارو عشق دا کھاون دے
مائے نی جہلم جاون دے
دلبر نے جدوں مکھ دکھلایا
سب کچھ بھلیا، ہوش گنوایا
مئے نوشی وچ سب کجھ پایا
دل دی پیاس بجھاون دے
مائے نی جہلم جاون دے
جہلم شہر دے کریں نظارے
جتھے رہندے دلبر پیارے
قادری اوتھے چین قرار اے
اج رج کے درشن پاون دے
مائے نی جہلم جاون دے
In this article the role played by the Muslim religious scholars in the Pakistan Movement has also been discussed. The most prominent among such scholars were Molana Mazharuddin Malik, Molana Shabeer Ahmad Usmani, Molana Ashraf Ali Thanvi, Molana Zafar Ahmad Ansari, Mufti Muhammad Shafee, Molana Ikram Khan Bengali, Molana Ahmad Raza Khan Brailvi, Molana Naeem Uddin Muradabadi, Molana Azad Subhani, Molana Abdul Hamid Badauni, and MolanaAbul Ala Maududi. At the end, an analysis of the ideology of Pakistan has been presented in the light of the excerpts taken from various speeches and statements made by the Quaid during 1938 and 1948. It shows that the Quaid wanted to make Pakistan an Islamic state governed by the teachings of Allah Taala. He wanted to make it a model Islamic state to convince others to realize that the commandments of Allah are practicable and are a means of salvation from hurdles and hardships.
Intellectual disability (ID) is a lifelong condition with tremendous clinical and genetic heterogeneity, affecting 1-3% population worldwide. It is characterized by cognitive impairment as well as adaptive deficits originating before the age of 18 years. Severity of ID along with associated clinical manifestation, determines the need of support in affected individuals. Genetics and environment both equally contribute to its etiology. During last few years, successive large scale studies using next generation sequencing (NGS) technologies have added many new genes to the existing gene repertoire for ID. Carrying out research studies in the inbred populations will allow the identification of recessive genetic defects. Therefore present project was designed to elucidate the molecular basis of autosomal recessive intellectual disability (ARID) in Pakistani population which shows high consanguinity with estimates more than 50%. So as to achieve the objectives, eighty families with history of intellectual disability were recruited from different cities. Complete medical history, written informed consents and blood samples were collected from the participating individuals. Forty nine families were selected on the basis of pedigree structures and processed further for genetic characterization through linkage analysis, whole exome sequencing (WES) and Sanger sequencing. Linkage analysis was carried out to screen thirty seven families for the presence of reported ID loci. Two families PKMR288 and PKMR304 showed homozygous regions linked with known ARID loci MRT10/ MRT20 and MRT1 respectively. Mapping of known X chromosome loci revealed linkages in six ID families PKMR229, PKMR244, PKMR251, PKMR253, PKMR271 and PKMR297. Whole exome sequencing (WES) was performed on twelve selected families. After exome data analysis and variant prioritization, pathogenic variants were identified in seven families. A reported frameshift mutation in ASPM gene was segregating in PKMR62 whereas a novel missense mutation in known THOC6 gene was detected in PKMR427. Potentially novel candidate ARID genes containing missense mutations were found in four families: EHBP1L1 in PKMR198, AREL1 in PKMR258, TM2D3 in PKMR325 and PRKAR2B in PKMR326. There was one family PKMR425 with missense mutation identified in FOXO4, a novel candidate gene for X-linked ID. Sanger sequencing was used to confirm these mutations and subsequently their co-segregation with ID phenotype in respective families. Mutation detection by means of high-throughput exome sequencing proved itself to be a cost-effective and time-saving approach. All the novel candidate genes were found to be implicated in different biological pathways related directly or indirectly to the brain growth and activity through in silico analysis. These findings will expand the existing database for genes involved in ARID, and will provide new insights into the molecular mechanisms of neurodevelopment leading to advancements in cognitive diagnostics and therapeutics.