Suchergebnisse - "Mandal, Kausik"

PubPharm (7)

1

MPV17 mutation-related mitochondrial DNA depletion syndrome : A case series in infants

enthalten in: Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology | 2023

von Samanta, A. | Srivastava, A. | Mandal, K. | +2

2

MPV17 mutation–related mitochondrial DNA depletion syndrome: A case series in infants

enthalten in: Indian journal of gastroenterology | 2023

von Samanta, A. | Srivastava, A. | Mandal, K. | +2

3

MPV17 mutation–related mitochondrial DNA depletion syndrome: A case series in infants

enthalten in: Indian journal of gastroenterology | 2023

von Samanta, A. | Srivastava, A. | Mandal, K. | +2

4

MPV17 mutation–related mitochondrial DNA depletion syndrome: A case series in infants

enthalten in: Indian Journal of Gastroenterology | 2023

von Samanta, A. | Srivastava, A. | Mandal, K. | +2

5

Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder : the East India Tubulopathy Gene Study

enthalten in: Pediatric nephrology (Berlin, Germany) | 2022

von Sinha, R. | Pradhan, S. | Banerjee, S. | +13

6

Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study

enthalten in: Pediatric nephrology | 2022

von Sinha, R. | Pradhan, S. | Banerjee, S. | +13

7

Whole-exome sequencing and variant spectrum in children with suspected inherited renal tubular disorder: the East India Tubulopathy Gene Study

enthalten in: Pediatric nephrology | 2022

von Sinha, R. | Pradhan, S. | Banerjee, S. | +13

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