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Phenylalanine hydroxylase gene mutations in phenylketonuria patients from India: identification of novel mutations that affect PAH RNA. [electronic resource] by
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- Chaudhary, Ajay K
- Reddy, E Chandrakanth
- Devi, A Radha Rama
- Savithri, G R
- Ratheesh, R
- Bashyam, Leena
- Mahesh, E
- Sen, Dity
- Puri, Ratna
- Verma, Ishwar C
- Verma, Inder C
- Nampoothiri, Sheela
- Vaidyanathan, Sunitha
- Chandrashekar, Mataguru D
- Kantheti, Prameela
Producer: 20100708
In:
Molecular genetics and metabolism vol. 100
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Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites. [electronic resource] by
- Straniero, Letizia
- Rimoldi, Valeria
- Soldà, Giulia
- Mauri, Lucia
- Manfredini, Emanuela
- Andreucci, Elena
- Bargiacchi, Sara
- Penco, Silvana
- Gesu, Giovanni P
- Del Longo, Alessandra
- Piozzi, Elena
- Asselta, Rosanna
- Primignani, Paola
Producer: 20160412
In:
Journal of human genetics vol. 60
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Selective dendrite-targeting of mRNAs of NR1 splice variants without exon 5: identification of a cis-acting sequence and isolation of sequence-binding proteins. [electronic resource] by
- Pal, Ranu
- Agbas, Abdulbaki
- Bao, Xiaodong
- Hui, Dongwei
- Leary, Cynthia
- Hunt, John
- Naniwadekar, Ashutosh
- Michaelis, Mary L
- Kumar, Keshava N
- Michaelis, Elias K
Producer: 20040210
In:
Brain research vol. 994
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