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WFS1 Gene-associated Diabetes Phenotypes and Identification of a Founder Mutation in Southern India
by
Chapla, Aaron
,
Johnson, Jabasteen
,
Korula, Sophy
,
Mohan, Nisha
,
Ahmed, Anish
,
Varghese, Deny
,
Rangasamy, Parthiban
,
Ravichandran, Lavanya
,
Jebasingh, Felix
,
Kumar Agrawal, Krishna
,
Somasundaram, Noel
,
Hesarghatta Shyamasunder, Asha
,
Mathai, Sarah
,
Simon, Anna
,
Jha, Sujeet
,
Chowdry, Subhankar
,
Venkatesan, Radha
,
Raghupathy, Palany
,
Thomas, Nihal
Published in
The journal of clinical endocrinology and metabolism
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The Journal Of Clinical Endocrinology And Metabolism
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Analysis
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Deafness
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Didmoad
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Dna Sequencing
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Endocrinology & Metabolism
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Female
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Founder Mutation
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Genes
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Genetic Screening
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Humans
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India - Epidemiology
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Life Sciences & Biomedicine
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Male
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Medical Screening
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Membrane Proteins - Genetics
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Mutation
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Next-Generation Sequencing
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Nucleotide Sequencing
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Oxford Journals Online
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Ezb-Free-00999 Freely Available Ezb Journals
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